Pharma PCD Franchise

Approx. Rs 650 / Strip Get Latest Price

Composition

Each film coated tablet contains Cefuroxime Axetil 500 mg

Description

Cefuroxime is a semisynthetic, broad-spectrum cephalosporin for oral administration. Cefuroxime inhibits bacterial cell wall synthesis by binding to one or more of the -binding proteins (PBPs) which in turn inhibits the final transpeptidation step of peptidoglycan synthesis in bacterial cell walls, thus inhibiting cell wall biosynthesis. Bacteria eventually lyse due to ongoing activity of cell wall autolytic enzymes (autolysins and murein hydrolases) while cell wall assembly is arrested.

Indications

URTI & ENT infection: e.g. Otitis media, sinusitis, tonsillitis and pharyngitis LRTI: Pneumonia, acute bronchitis and acute exacerbation of chronic bronchitis Genito–urinary tract infection: e.g. Cystitis, urethritis, pyelonephritis Gonorrhoea, acute uncomplicated gonococcal urethritis and cervicitis Skin and soft tissue infections: e.g. Pyoderma, impetigo and furenculosis

Dosage and administration

The usual course of therapy is 7 days (range 5-10 days). For optimal absorption Saloxim-500 be taken with food.

• Pharyngitis/Tonsillitis 250 mg b.i.d.

• Acute bacterial maxillary sinusitis 250 mg b.i.d.

• Acute exacerbation of chronic bronchitis 250-500 mg b.i.d.

• Acute bronchitis 250 mg b.i.d.

• Uncomplicated UTI 250 mg b.i.d.

• Pyelonephritis 250 mg b.i.d.

• Uncomplicated skin & skin structure infections 250-500 mg b.i.d.

• Uncomplicated gonorrhoea 1000 mg single dose

Contraindications

Patients with known hypersensitivity to cephalosporin antibiotics

Presentation

Saloxim-500 Tablets

Strip of 10 Tablets

Approx. Rs 270 / Strip Get Latest Price

Cefixime-Clav is indicated for the treatment of:

• Uncomplicated Urinary Tract Infections
• Otitis Media
• Pharyngitis and Tonsillitis
• Acute Bronchitis and Acute Exacerbations of Chronic Bronchitis
• Uncomplicated gonorrhea (cervical/urethral)

We are looking for Pharma PCD & Pharma franchisee queries from all over India. 

"Third party inquiries are also solicited"

Approx. Rs 190 / Strip Get Latest Price

SALVICA-OF TABLETS

Cefixime…… 200 mg

Ofloxacin IP…200 mg

CLINICAL PHARMACOLOGY

Cefixime:

Pharmacokinetic Actions

Cefixime is absorbed after oral administration and has a bioavailability of about 40% to 50%.

Its protein binding is approximately 60% with an average half-life of 3 to 4 hours.

The distribution volume is 3.5 l/kg and total clearance is approximately 15 l/h. The half-life in plasma is 10-1 2 hours and gives a 24 hour effect after dosing once daily. Its excretion is through renal and biliary route.

Ofloxacin:

Pharmacokinetic Actions

It is absorbed after oral administration and has a bioavailability of about 50 to 70%.

Its protein binding is approximately 60% wEth an average half-life of 0.75 to 1 hours.

Its excretion is through renal route.

MECHANISM OF ACTION:

Cefixime: It is bactericidal beta-lactam antibiotic (such as penicillins). Cefixime disrupt the synthesis of the peptidoglycan layer of bacterial cell walls. The peptidoglycan layer is important for cell wall structural integrity. The final transpeptidation step in the synthesis of the peptidoglycan is facilitated by transpeptidases known as penicillin-binding proteins (PBPs). PBPs bind to the D-Ala-D-Ala at the end of muropeptides (peptidoglycan precursors) to crosslink the peptidoglycan.

Ofloxacin: Ofloxacin is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria. It functions by inhibiting DNA gyrase, a type II topoisomerase, and topoisomerase IV, which is an enzyme necessary to separate replicated DNA, thereby inhibiting cell division. The fluoroquinolones interfere with DNA replication by inhibiting an enzyme complex called DNA gyrase. This can also affect mammalian cell replication.

Recent studies have demonstrated a correlation between mammalian cell cytotoxicity of the quinolones and the induction of micronuclei. As such some fluoroquinolones may cause injury tothe chromosome of eukaryotic cells.
We are looking for Pharma PCD & Pharma franchisee queries from all over India. 

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Mypod 100/200mg Tablets

Cefpodoxime - A third generation cephalosporin .

Cefpodoxime proxetil is used orally for the treatment of mild to moderate respiratory tract infections (i.e., acute exacerbations of chronic bronchitis, acute maxillary sinusitis, community-acquired pneumonia) caused by susceptible bacteria; the treatment of acute otitis media caused by susceptible bacteria; and the treatment of pharyngitis and tonsillitis caused by Streptococcus pyogenes (group A β-hemolytic streptococci). The drug also is used orally for the treatment of uncomplicated gonorrhea and for the treatment of mild to moderate uncomplicated skin and skin structure or uncomplicated urinary tract infections caused by susceptible bacteria.

Prior to initiation of cefpodoxime proxetil therapy, appropriate specimens should be obtained for identification of the causative organism and in vitro susceptibility tests. Cefpodoxime proxetil may be started pending results of susceptibility tests but should be discontinued if the organism is found to be resistant to the drug.

 

Acute Otitis Media

Pharyngitis and Tonsillitis

Respiratory Tract InfectionsAcute Exacerbations of Chronic Bronchitis

Acute Sinusitis

Community-acquired Pneumonia

Skin and Skin Structure Infections

Urinary Tract Infections

Gonorrhea and Associated InfectionsUncomplicated Gonorrhea

Disseminated Gonococcal Infections

 

Approx. Rs 1,170 / Unit Get Latest Price

Generic Name: Meropenem Brand Name: Meronu 1g Drug Class And Mechanism: Meropenem is an injectable carbapenem antibiotic. It is similar to impenem and cilastin (Primaxin). Meropenem prevents bacteria from forming the walls that surround them. The walls are necessary to protect bacteria from their environment and to keep the contents of the bacterial cell together. Bacteria cannot survive without a cell wall. Meropenem is effective against susceptible strains of E. coli, H. influenzae, K. pneumoniae, N. meningitidis, P. aeruginosa, and many other bacteria. The FDA approved meropenem in June 1996. Prescribed For:  Meropenem is used to treat infections such asbacterial meningitis, abdominal infections, and complicated skin and soft tissue infections caused by susceptible organisms.

Approx. Rs 258 / Strip Get Latest Price

Uses of Linezolid 600mg + Cefixime 200mg:

Linezolid Is An Anti-Biotic And Is Used In The Treatment Of Various Bacterial Infections , For Example,Pneumonia, Skin Infections, And Infections That Are Resistant To Other Antibiotics. Linezolid And Cefixime Combination Is Used In The Treatment Of Typhoid And Few Other Respiratory Infections.

 

STRIP OF 6 TAB

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SALOF-OZ PLUS TABS Ofloxacin I.P. 200 mg Ornidazole I.P. 500 mg Lactic Acid Bacillus 120 Million spores. Saccharomyces Boulardii 2 Million spores. INDICATIONS Diarrhea GI Infections Dysentry Abdominal pain Traveler's diarrhea Lactose Intolerance Ofloxacin Offers broad spectrum of activity against gastrointestinal pathogens including Escherichia Coil and species of Salmonella, Shigella, Campylobacter Yersinia, Plesiomonas, Aeromonas and vibrio. A total cure achieved in 96.5% of cases with diarrhoea and in 100% of cases with dysentery. Ornidazole Combination of ofloxacin with ornidazole significantly reduces number of watery stool and associated symptoms like nausea,abdominal pain. Shows tolerability rate of 98.43%. Lactic Acid Bacillus Helps in normalising intestinal flora elicits positive results in treating acute infections diarrhoea. Alleviates bacterial/viral induced diarrhoea espically in infants. Saccharomyces Boulardii Significantly reduces the duration of diarrhea from -26.05 to -13.34,stool frequency -1.38 to -0.10 after intervention compared with control. Inhibits neutralizes bacterial virulence factors.

Approx. Rs 368 / Strip Get Latest Price

Linzosal-600 Tablets
Eact tablet contains
Linezolid 600mg; tabs.

INDICATIONs

Susceptible vancomycin-resistant E. faecium (VREF) infections, nosocomial and community-acquired pneumonia, complicated skin and skin structure infections (including diabetic foot infections) without osteomyelitis, uncomplicated skin and skin structure infections.

Adult

Infuse inj over 30-120 mins; switch to oral form when appropriate. VREF 600mg every 12hrs for 14-28 days. Pneumonia, complicated skin and skin structure 600mg every 12hrs for 10-14 days. Uncomplicated skin and skin structure (oral forms only) 12-17yrs 600mg every 12hrs; >17yrs 400mg every 12hrs; both for 10-14 days. MRSA 600mg every 12hrs.

Children

Infuse inj over 30-120 mins; switch to oral form when appropriate. Neonates

Contraindications

During or within 2 weeks of MAOIs (eg, phenelzine, isocarboxazid).

Warnings/Precautions

Not for treating catheter-related bloodstream infections or catheter-site infections. Uncontrolled hypertension, pheochromocytoma, thyrotoxicosis, carcinoid syndrome not recommended. History of seizures. Monitor CBC's weekly (esp. if otherwise at risk). Consider discontinuing if myelosuppression occurs or worsens. Therapy >28 days. Peripheral and optic neuropathy. Monitor visual function if treatment 3 months and if new visual symptoms occur. Diabetes; monitor for hypoglycemia, if occurs, reduce dose or discontinue. Pregnancy (Cat.C). Nursing mothers.

Interactions

See Contraindications. Concomitant sympathomimetics (eg, ), vasopressive agents (eg, epinephrine, norepinephrine), dopaminergics (eg, dopamine, dobutamine) not recommended. Risk of serotonin syndrome with concomitant SSRIs, trycyclic antidepressants, triptans, , bupropion, or buspirone. Avoid large amounts of dietary tyramine (keep

Approx. Rs 60 / Bottle Get Latest Price

Description:

• Salof-OZ has in vitro activity against a broad spectrum of gram-positive and gram-negative aerobic and anaerobic bacteria. Ofloxacin is thought to exert a bactericidal effect on susceptible microorganisms by inhibiting DNA gyrase, an essential enzyme that is a critical catalyst in the duplication, transcription, and repair of bacterial DNA.Ofloxacin has been shown to be active against most strains of the following microorganisms both in vitro and in specific clinical infections.

Gram-positive Aerobes:

• Staphylococcus aureus, Streptococcus pneumoniae, and Streptococcus pyogenes.

Gram-negative Aerobes:

• Citrobacter diversus, Enterobacter aerogenes, Escherichia coli, Haemophilus influenzae, Klebsiella pneumoniae, Neisseria gonorrhoeae, Proteus mirabilis, Pseudomonas aeruginosa

Other:

• Chlamydia trachomatis.Ornidazole is a 5-nitroimidazole derivative with actions similar to Metronidazole and Tinidazole and is used in the treatment of susceptible Protozoal Infections and also in Anaerobic Bacterial Infections.It is effective against Protozoa including Entamoeba histolytica, Giardia lambia and Trichomonas spp and Bacteria such as Bacteriodes spp., Anaerobic cocci, Fusobacterium spp., Clostridum spp., and Gardenerlla vaginalis. It acts by damage of DNA strands or inhibition of their synthesis.Both Ofloxacin and Ornidazole are almost completely absorbed from the small intestine when administered orally both having almost 100% bioavailability. Subsequent plasma concentrations of Ofloxacin are obtained in 1-2 hours after oral administration. Peak plasma concentrations of Ornidazole are obtained within 2 hours of administration.The plasma elimination of Ornidazole is 12 to 15 hours and less than 15% is bound to plasma proteins. It is widely distributed in body tissues and fluids. Ornidazole is metabolised in the liver and is excreted in the urine mainly as metabolites and conjugates and to a lesser extent in the faces.

Indications:

• Salof-OZ is indicated for the treatment of a wide variety of infections caused by susceptible gram-positive and gram-negative organisms along with anaerobes and protozoa. Gynaecological infections including prophylaxis in gynaecological surgeries. Surgical prophylaxis and surgical wound infections. Respiratory tract infections like lung abscess, aspiration pneumonia, empyema and bronchiectasis. ENT infections like chronic sinusitis, chronic suppurative otitis media, cholesteatoma and mastoiditis. Orofacial and dental infections.Dermatological infections like cellulitis, breast and other cutaneous abscesses, angrene, diabetic and decubitus ulcers.Intra-abdominal infections and diarrhoeas of mixed bacterial and protozoal origin.

Dosage:

• The usual adult dose is one tablet of Salof-OZ twice a day. The doses may be increased in severe infections. The duration of treatment depends upon the type and severity of infection.

Contraindications:

• Hypersensitivity to the quinolone group or the nitroimidazole group of compounds and in those patients with a history of blood dyscrasias.

Other Details:

• Each 5 ml contains
• Ofloxacin 50mg
• Ornidazole 125 mg

Approx. Rs 110 / Strip Get Latest Price

Cefpodoxim Proxetil is an extended spectrum, third generation cephalosporin . Bactericidal - Arrests the cell wall assembly leading to bacterial cell death. Ofloxacin is a chemotherapeutic of fluoroquinolone class. Bactericidal - Inhibits the super coiling activity of bacterial DNA gyrase, halting DNA replication

Uses:

• Upper Respiratory Tract Infection's Lower Respiratory Tract Infection's
• Urinary Tract Infection's Infection Caused by Bacteria
• Patients with High Fever 100 ° F Asthma, Smokers
• AECB Past History of TB

Approx. Rs 49 / Strip Get Latest Price

Our clients have been a huge inspiration behind the wide array of Ofloxacin Tablets offered by us. We follow the international standards of quality while testing these products. As per the needs and requirements of our clients, we can also customize the packaging quantities of these products.
Features:

Quick response

Precise composition

Longer shelf life

Zero side effects

High purity

Uses:

This medication is used to treat a variety of bacterial infections

Ofloxacin belongs to a class of drugs called quinolone

It works by stopping the growth of bacteria

This treats only bacterial infections

Specification:

Composition: Ofloxacin

Approx. Rs 427 / Unit Get Latest Price

PEMAX-TZ  INJ 4.5G

Piperacillin Sodium and Tazobactam for Injection (4g+500mg)

Description:
Piperacillin and Tazobactam for injection is an injectable antibacterial combination product consisting of the semisynthetic antibiotic piperacillin sodium and the beta-lactamase inhibitor tazobactam sodium for intravenous administration. 

Piperacillin sodium is derived from D(-)aminobenzyl-penicillin. The chemical name of piperacillin sodium is sodium (2S,5R,6R)-6-[(R)-2-(4-ethyl-2,3-dioxo-1-piperazine-carboxamido)-2-phenylacetamido]-3,3-dimethyl-7-oxo-4-thia-1azabicyclo[3.2.0]heptane-2-carboxylate. 

Tazobactam sodium, a derivative of the penicillin nucleus, is a penicillanic acid sulfone. Its chemical name is sodium (2S,3S,5R)-3-methyl-7-oxo-3-(1H-1,2,3-triazol-1-ylmethyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate-4,4-dioxide. 

Mechanism Of Action:
Inhibits bacterial cell wall synthesis by binding to one or more of the penicillin binding proteins (PBPs); which in turn inhibits the final transpeptidation step of peptidoglycan synthesis in bacterial cell walls, thus inhibiting cell wall biosynthesis. Bacteria eventually lyse due to ongoing activity of cell wall autolytic enzymes (autolysins and murein hydrolases) while cell wall assembly is arrested. Tazobactam inhibits many beta-lactamases, including staphylococcal penicillinase and Richmond and Sykes types II, III, IV, and V, including extended spectrum enzymes; it has only limited activity against class I beta-lactamases other than class Ic types.

Indications:

In adults and children over 12 years of age:

• Bacterial infections of the lungs and airways (chest or lower respiratory tract infections)
• Bacterial infections within the abdomen
• Bacterial infections of the urinary tract
• Bacterial infections of the skin
• Bacterial infections of the blood (septicaemia or blood poisoning)
• Bacterial infections in people with low white blood cell counts (neutropenia) and hence decreased ability to fight infection (used in combination with an aminoglycoside antibiotic for this purpose)

In children under 12 years of age:

• Appendicitis complicated by a burst appendix, peritonitis and/or abcess formation in children aged 2 to 12 years.
• Bacterial infections in children with low white blood cell counts (neutropenia) and hence decreased ability to fight infection (used in combination with an aminoglycoside antibiotic for this purpose)

Dosage And Administration:
PEMAX-TZ  INJ 4.5G should be administered by intravenous infusion over 30 minutes. 

Adults: The usual total daily dose of PEMAX-TZ  INJ 4.5G is 3.375 g every six hours totaling 13.5 g (12.0 g piperacillin/1.5 g Tazobactam). 
Contraindications: PEMAX-TZ  INJ 4.5G is contraindicated in patients with a history of allergic reactions to any of the penicillins, cephalosporins, or beta-lactamase inhibitors.

Important: The drug information on this Web page is meant to be educational. It is not a substitute for medical advice. Please see your health care professional for more information about your specific medical condition and the use of the above mentioned drug.

Approx. Rs 199 / Unit Get Latest Price

Garizone  1.5 G Inj Powder For Preparation Of Injection Solution (Sulbactam Cefoperazone For Injection)   Composition Each Vial contains: Sulbactam Sodium USP equivalent to Sulbactam : 500 mg Cefoperazone Sodium USP equivalent to Cefoperazone : 1000 mg   Indications The combination of Cefoperazone sodium and Sulbactam sodium is indicated for the treatment of the following infections caused by susceptible organisms.   Respiratory tract infections (Upper and Lower), Urinary Tract Infections, Peritonitis, Cholecystitis, Cholangitis and other intra-abdominal infections, Bacterial sinusitis, Meningitis, Skin and soft tissue infections, Bone and Joint infections, Pelvic Inflammatory disease - endometritis, gonorrhea and other infections of the genital tract.   Dosage and Administration Adults: The usual adult dose of the combination is 2 to 4 g/day (i.e, 1-2 g/day each of Cefoperazone and Sulbactam) given IV or IM in equally divided doses every 12 hours.   In severe or refractory infections the daily dosage may be increased to 8g (i.e, 4g/day each of Cefoperazone and Sulbactam) given IV in equally divided doses every 12 hours. The recommended maximum daily dosage of Sulbactam is 4g (8g of the combination).   Dosage regimens should be adjusted in patients with marked decrease in renal function.   Children: The usual dosage in children is 40-80mg/kg/day (20 to 40 mg/kg/day each of Cefoperazone and Sulbactam) every six to twelve hours. In serious or refractory infections, these dosages may be increased up to 160 mg/kg/idea of the combination. (i.e., 80 mg/kg/day each of Cefoperazone and Sulbactam) every six to twelve hours.   Contraindications Allergy to Penicillin or Cephalosporin.   Presentation Vial of 1.5 gm with Water for Injection

Approx. Rs 78 / Bottle Get Latest Price

Salvica-of Tablets

Cefixime…… 200 mg….. β lactam antibiotics (Third generation cephalosporin antibiotic)

Ofloxacin IP…200 mg…. Second-generation fluoroquinolone

 

Clinical Pharmacology

Cefixime:

Pharmacokinetic Actions

Cefixime is absorbed after oral administration and has a bioavailability of about 40% to 50%.

Its protein binding is approximately 60% with an average half-life of 3 to 4 hours.

The distribution volume is 3.5 l/kg and total clearance is approximately 15 l/h. The half-life in plasma is 10-1 2 hours and gives a 24 hour effect after dosing once daily. Its excretion is through renal and biliary route.

Ofloxacin:

Pharmacokinetic Actions

It is absorbed after oral administration and has a bioavailability of about 50 to 70%.

Its protein binding is approximately 60% wEth an average half-life of 0.75 to 1 hours.

Its excretion is through renal route.

Mechanism Of Action:

Cefixime: It is bactericidal beta-lactam antibiotic (such as penicillins). Cefixime disrupt the synthesis of the peptidoglycan layer of bacterial cell walls. The peptidoglycan layer is important for cell wall structural integrity. The final transpeptidation step in the synthesis of the peptidoglycan is facilitated by transpeptidases known as penicillin-binding proteins (PBPs). PBPs bind to the D-Ala-D-Ala at the end of muropeptides (peptidoglycan precursors) to crosslink the peptidoglycan.

Ofloxacin: Ofloxacin is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria. It functions by inhibiting DNA gyrase, a type II topoisomerase, and topoisomerase IV, which is an enzyme necessary to separate replicated DNA, thereby inhibiting cell division. The fluoroquinolones interfere with DNA replication by inhibiting an enzyme complex called DNA gyrase. This can also affect mammalian cell replication.

Recent studies have demonstrated a correlation between mammalian cell cytotoxicity of the quinolones and the induction of micronuclei. As such some fluoroquinolones may cause injury tothe chromosome of eukaryotic cells.

Approx. Rs 165 / Unit Get Latest Price

Cefixime 200 with Lactobacillus 60 Million Spores
We Salveo Lifecare, are one of the prominent suppliers of a wide range of Pharmaceutical Drugs. Our wide range includes Capsule, Soft gels, Tablets, SACHET, Injections, dry Syrups, ayurvedic preparations and Syrups.

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Azisal 250/500 Tablets
Each Film Coated Tablet Contains:
Composition:
Azithromycin IP 250 / 500 mg
Azithromycin (AZT) is macrolide antibiotics, it is an Azalide. It inhibits protein synthesis by binding 50S ribosomal subunit of the bacteria.
Indications:

Otitis media

Respiratory tract infection

Cystic fibrosis

Anti-inflammatory in COPD Patient

In P. Falciparum Malaria with other Antimalarial drugs

Typhoid fever

Neissaria gonorrhoeae.

Product Description:

A new combination of cefixime and azithromycin with Lactobacillus is used for the treatment of upper and lower respiratory tract infection. Cefixime, an antibiotic, is a third-generation cephalosporin like ceftriaxone and cefotaxime. Cefixime is highly stable in the presence of beta-lactamase enzymes. As a result, many organisms resistant to penicillins and some cephalosporins due to the presence of beta-lactamases, may be susceptible to cefixime. Whereas Azithromycin due to it's long half life, which enables once daily dosing and shorter administration durations, is a property distinct from other macrolides.

Pharmacology:
Azithromycin:
Absorption:
Following oral administration, azithromycin is rapidly absorbed and widely distributed throughout the body. Bioavailability is 37% following oral administration. Absorption is not affected by food.
Distribution:
Azithromycin is extensively distributed in tissues with tissue concentrations reaching up to 50 times greater than plasma concentrations. Drug becomes concentrated within macrophages and polymorphonucleocytes giving it good activity against Chlamydia trachomatis.
Elimination:
Biliary excretion of azithromycin, predominantly as unchanged drug, is a major route of elimination. The Half life being 68 hours.
Mechanism of Action:
Azithromycin inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit of the bacterial 70S ribosome. Binding inhibits peptidyl transferase activity and interferes with amino acid translocation during the process of translation. Its effects may be bacteriostatic or bactericidal depending of the organism and the drug concentration.
Adverse Effects:

Diarrhea that is watery or bloody.

Chest pain, uneven heartbeats.

Nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes).

Severe skin reaction - fever, sore throat, swelling in your face or tongue, burning in your eyes, skin.
Contraindications:
Known hypersensitivity to cefixime or other cephalosporins. Contraindicated in patients with a history of liver disease, kidney disease and also muscle disease.

Approx. Rs 147.5 / Piece Get Latest Price

Our huge team of skilled and trained professionals have enabled us to provide a huge gamut of Co - Amoxiclav 1.2 g Injection. We always test these products for quality to keep up with the industrial standards.These products are packed in varied quantities as per the requirements and demands of the clients. 

Features:
•Quick response
•Precise composition
•Longer shelf life
•Zero side effects
•High purity  
Indications:
•Upper respiratory tract, such as sinusitis, otitis media, tonsillitis
•Lower respiratory tract, such as bronchitis pneumonia
•Urinary tract infections, such as cystitis, urethritis, pyelonephritis
•Skin and soft tissues   Contra-Indications:
•Allergy to penicillins and cephalosporins
•Safety in pregnancy has not been established
•Leoklav is contra-indicated in patients with a previous history of Leoklav associated jaundice/hepatic dysfunction
•Safety and efficacy in children has not been established with the parenteral forms of Leoklav
:
•Quick response
•Precise composition
•Longer shelf life
•Zero side effects
•High purity  
Indications:
•Upper respiratory tract, such as sinusitis, otitis media, tonsillitis
•Lower respiratory tract, such as bronchitis pneumonia
•Urinary tract infections, such as cystitis, urethritis, pyelonephritis
•Skin and soft tissues   Contra-Indications:
•Allergy to penicillins and cephalosporins
•Safety in pregnancy has not been established
•Leoklav is contra-indicated in patients with a previous history of Leoklav associated jaundice/hepatic dysfunction
•Safety and efficacy in children has not been established with the parenteral forms of Leoklav

Approx. Rs 290 / Strip Get Latest Price

Description:

• Our huge range of products includes a wide array of Cefpodoxime and Clavulanic Acid Tablets that is quite popular among our clients. We have the acumen to test these products as per the international standards of quality to ensure non contamination and long shelf life. We can also customize the packaging quantities of these products if the clients requests.

Features:

• Accurate composition
• Effectiveness
• Safety
• Pure
• Quality-assured

Uses:

• It used for the treatment of urinary tract infections, pneumonia, bronchitis, gonorrhea and multiple other infections

Specification:

• Composition: Cefpodoxime clavulanic acid

Approx. Rs 82 / Pack Get Latest Price

Description:

• We are also the leading trader and supplier of a huge range of Levofloxacin Tablets 500 Mg. These products are offered to our clients in varied packaging quantities as per their needs and guidelines. Tested in accordance to the international standards of quality, these products are very pure and have a long life span.

Features:

• Quick response
• Precise composition
• Longer shelf life
• Zero side effects
• High purity
• High effectiveness

Specification:

• Composition: Levofloxacin

Uses:

• Treatment to Prevent Anthrax following Exposure to Disease
• Acute Inflammation of the Maxillary Sinus
• Acute Maxillary Sinus S. Pneumoniae Bacteria Infection
• Acute Maxillary Sinus H. Influenzae Bacteria Infection
• Acute Maxillary Sinus M. Catarrhalis Bacteria Infection
• Pneumonia caused by Pneumococcus Bacteria
• Bacterial Pneumonia caused by Haemophilus Influenzae, Pneumonia due to the Bacteria Haemophilus Parainfluenzae, Bacterial Pneumonia caused by Strep
• Bacterial Pneumonia caused by Staphylococcus
• Pneumonia due to Methicillin-Sensitive

Information provided at this web site is of a general nature and is not intended to take the place of a physician's advice. It is vital that persons diagnosed with, or suspected of having, any disease consult with their physician to assure proper evaluation, treatment and interpretation of information contained on this site.

Approx. Rs 298 / Piece Get Latest Price

we are looking for pharma pcd & pharma franchisee queries from all over india.

"third party inquiries are also solicited"

clindamycin injection is used to treat certain types of bacterial infections, including infections of the lungs, skin, blood, bones, joints, female reproductive organs, and internal organs. clindamycin is in a class of medications called lincomycin antibiotics. it works by slowing or stopping the growth of bacteria. antibiotics such as clindamycin will not kill the viruses that cause colds, flu, and other viral infections.

Approx. Rs 180 / Strip Get Latest Price

Description:

• We have the acumen to become the leading supplier and trader of Cefpodoxime 200 Mg Tablets. The packaging quantities of these products are traded keeping in mind the various needs and requirements of our respected clients. Our team is constantly involved in the testing of these products as per the international standards of quality to ensure that it does not falter at the time of operation.  

Features:

• Quick response
• Precise composition
• Longer shelf life
• Zero side effects
• High purity

Uses:

• It used for the treatment of urinary tract infections, pneumonia, bronchitis, gonorrhea, and multiple other infections  

Specification:

• Composition: Cefpodoxime 200 mg

Approx. Rs 80 / Strip Get Latest Price

Since the time we formulated our company we are known in the market for the range of Ofloxacin & Ornidazole Tablets. We can also customize the packaging quantities of these products as per the needs and requirements of our clients. Our team of skilled and trained professionals are involved in the testing of these products as per the international standards of quality.

Features:

• Quick response
• Precise composition
• Longer shelf life
• Zero side effects
• High purity
• High effectiveness

Specification:

• Composition: Ofloxacin & Ornidazole Uses: Ofloxacin-
• Typhoid fever
• Pneumonia Ornidazole-
• Anaerobic infections both pre & post operatively
• Bacterial vaginosis
• Amoebic dysentery
• Amoebic liver abscess
• Hepatic and intestinal amoebiasis
• Other protozoan infection like Giardiasis, Trichomoniasis

Approx. Rs 238 / Strip Get Latest Price

Each Film Coated Tablet Contains:

Composition:

• Cefixime Trihydrate IP
• Eq. to Anhydrous Cefixime :200 mg
• Azithromycin IP  : 250 mg

Cefixime Trihydrate is an orally active antibiotic with similar antibacterial spectrum and resistance to β-lactamase as third generation cephalosporins. It inhibits an enzyme transpeptidase which is responsible for bacterial cell walls synthesis.

Azithromycin (AZT) is macrolide antibiotics, it is [9-de-oxy-9a-aza-9a-methyl-9a-homoerythromycin A dihydrate] is an Azalide. It inhibits protein synthesis by binding 50S ribosomal subunit of the bacteria.

Indications:

Cefixime Trihydrate:

•   Lower Respiratory Tract Infections
•   Pharyngitis and tonsilitis
•   Acute sinusitis
•   Gnorrhea and associated infections
•   Acute Urinary Tract Infections
•   Acute Otitis Media
•   Helicobacter pylori infection
•   Lyme disease
•   Salmonlella and shigella infections.

Azithromycin:

•   Otitis media
•   Respiratory tract infection
•   Cystic fibrosis
•   Anti-inflammatory in COPD Patient
•   In P. Falciparum Malaria with other Antimalarial drugs
•   Typhoid fever
•   Neissaria gonorrhoeae.

Rationale of Combination:

Product Description:

A new combination of cefixime and azithromycin with Lactobacillus is used for the treatment of upper and lower respiratory tract infection. Cefixime, an antibiotic, is a third-generation cephalosporin like ceftriaxone and cefotaxime. Cefixime is highly stable in the presence of beta-lactamase enzymes. As a result, many organisms resistant to penicillins and some cephalosporins due to the presence of beta-lactamases, may be susceptible to cefixime. Whereas Azithromycin due to it's long half life, which enables once daily dosing and shorter administration durations, is a property distinct from other macrolides.

Pharmacology:

Cefixime Trihydrate:

Absorption: About 40% to 50% is absorbed. C maxfollowing 200 and 400 mg doses of oral suspension are 3 and 4.6 mcg/mL, respectively. T max occurs between 2 and 6 h following administration of 400 mg and between 2 and 5 h after a 200 mg dose.

Distribution: Protein binding is about 65%.
Elimination About 50% of absorbed dose is excreted unchanged in the urine in 24 h. Serum t ½averages 3 to 4 h, but may be as long as 9 h in some healthy subjects.


Azithromycin:

Absorption: Following oral administration, azithromycin is rapidly absorbed and widely distributed throughout the body. Bioavailability is 37% following oral administration. Absorption is not affected by food.

Distribution: Azithromycin is extensively distributed in tissues with tissue concentrations reaching up to 50 times greater than plasma concentrations. Drug becomes concentrated within macrophages and polymorphonucleocytes giving it good activity against Chlamydia trachomatis.

Important: The drug information on this Web page is meant to be educational. It is not a substitute for medical advice. Please see your health care professional for more information about your specific medical condition and the use of the above mentioned drug

Approx. Rs 140 / Strip Get Latest Price

Salvica-of Tablets Cefixime…… 200 mg….. β lactam antibiotics (Third generation cephalosporin antibiotic) Ofloxacin IP…200 mg…. Second-generation fluoroquinolone   Clinical Pharmacology Cefixime: Pharmacokinetic Actions Cefixime is absorbed after oral administration and has a bioavailability of about 40% to 50%. Its protein binding is approximately 60% with an average half-life of 3 to 4 hours. The distribution volume is 3.5 l/kg and total clearance is approximately 15 l/h. The half-life in plasma is 10-1 2 hours and gives a 24 hour effect after dosing once daily. Its excretion is through renal and biliary route. Ofloxacin: Pharmacokinetic Actions It is absorbed after oral administration and has a bioavailability of about 50 to 70%. Its protein binding is approximately 60% wEth an average half-life of 0.75 to 1 hours. Its excretion is through renal route. Mechanism Of Action: Cefixime: It is bactericidal beta-lactam antibiotic (such as penicillins). Cefixime disrupt the synthesis of the peptidoglycan layer of bacterial cell walls. The peptidoglycan layer is important for cell wall structural integrity. The final transpeptidation step in the synthesis of the peptidoglycan is facilitated by transpeptidases known as penicillin-binding proteins (PBPs). PBPs bind to the D-Ala-D-Ala at the end of muropeptides (peptidoglycan precursors) to crosslink the peptidoglycan. Ofloxacin: Ofloxacin is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria. It functions by inhibiting DNA gyrase, a type II topoisomerase, and topoisomerase IV, which is an enzyme necessary to separate replicated DNA, thereby inhibiting cell division. The fluoroquinolones interfere with DNA replication by inhibiting an enzyme complex called DNA gyrase. This can also affect mammalian cell replication. Gram-positive Organisms. •  Streptococcus Pneumoniae, •  Streptococcus Pyo Genes. • Gram-negative Organisms. •  Haemophilus Influenzae •  (beta-lactamase Positive And Negative Strains), •  Moraxefia (branhamefia) Catanhalis (most Of Which Are Beta­lactamase Positive),  Escherichia Coli,  Proteus Mirabilis, Neisseria Gonorrhoeae (including Penicillinase And Non­peniainase Producing Strains).  Cefixime Has Been Shown To Be Active In Vitro Against Most Strains Of The Following Organisms; However, Clinical Efficacy Has Not Been Established. Packing: Strip of  10 tablets Important: The drug information on this Web page is meant to be educational. It is not a substitute for medical advice. Please see your health care professional for more information about your specific medical condition and the use of the above mentioned drug

Approx. Rs 290 / Strip Get Latest Price

Salvica-CV Feature: • Each Tablet Contains • Cefixime 200 mg • Clavulanic Acid 125 mg  Cefixime which possesses excellent efficacy against a broad spectrum of pathogens, including Haemophilus influenzae, Streptococcus pneumoniae and Moraxella catarrhalis. It is important first-line choice against common bacterial infections.

Approx. Rs 170 / Strip Get Latest Price

Saltip 625 Tablets Each film-coated tablet contains Amoxycillin trihydrate IP equivalent to Amoxycillin 500 mg and Clavulanic Acid 125 mg (Present as Clavulanate Potassium USP)   Saltip Dry Syrup Each 5ml (on reconstitution contains) Amoxycillin trihydrate IP equivalent to Amoxycillin 200 mg and Clavulanate Potassium USP equivalent to Clavulanic Acid 28.5 mg   Description Saltip is an oral antibacterial combination consisting of the semisynthetic antibiotic amoxycillin and the ß -lactamase inhibitor, clavulanate potassium (the potassium salt of clavulanic acid). Amoxycillin is a semi-synthetic penicillin which exerts its bactericidal action by inhibition of cell wall synthesis. Clavulanic acid is produced by the fermentation of Streptomyces clavuligerus. It is a ß -lactam structurally related to the penicillins and possesses the ability to inactivate a wide variety of ß -lactamases by blocking the active sites of these enzymes. Clavulanic acid is particularly active against the clinically important plasmid-mediated ß -lactamases frequently responsible for transferred drug resistance to penicillins and cephalosporins.   Indications Saltip is indicated in the treatment of infections caused by susceptible strains in the conditions listed below: • Otitis Media • Sinusitis • Skin and Skin Structure Infections • Urinary Tract Infections   Dosage and administration Adults: The usual adult dose is one 625 mg tablet of Saltip every 12 hours or one 375 mg tablet every 8 hours. For more severe infections and infections of the respiratory tract, the dose should be one 625mg tablet every 8 hours. Pediatric Patients: Pediatric patients weighing 40 kg or more should be dosed according to the adult recommendations.   Contraindications • Patients with a history of allergic reactions to any penicillin. • Patients with a previous history of cholestatic jaundice/hepatic dysfunction   Presentation • Saltip 625 Tablets • Strip of 10 tablets • Saltip Dry Syrup • 30 ml bottle

Approx. Rs 1,358 / Unit Get Latest Price

Cilaric Inj 1g

Imipenem and Cilastatin Injection

Generic Name: imipenem and cilastatin sodium
Dosage Form: injection, powder, for solution

To reduce the development of drug-resistant bacteria and maintain the effectiveness of imipenem and cilastatin for injection (I.V.) and other antibacterial drugs, imipenem and cilastatin for injection (I.V.) should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.

For Intravenous Injection Only

 

Approx. Rs 168 / Strip Get Latest Price

Salvica-OZ Tablets

Each Tablets contains

Cefixime         200 mg

Ornidazole       500 mg

SALVICA-OZ Tablets contains Cefixime and Ornidazole.

It is highly stable in the presence of beta-lactamase enzymes. The antibacterial effect of Cefixime results from inhibition of mucopeptide synthesis in the bacterial cell wall. Cefixime binds to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall, causing the inhibition of the third and last stage of bacterial cell wall synthesis.

ORNIDAZOLE contains an imidazole ring which bears a nitro group. It is an anti-amoebic agent. Ornidazole has a broad spectrum -cidal activity against Protozoa and some anaerobic bacteria.

Cefixime is an antibiotic, third-generation cephalosporin. Ornidazole belongs to the class of nitroimidazoles.

SALVICA-OZ Tablets are used in the treatment of the following conditions:

• Diarrhea and dysentery
• Abdominal infections
• Dental infections
• Post-surgical infections
• Infections of female reproductive tract

 

Salvica-OZ (Cefixime Trihydrate 200mg+ Ornidazole 500mg Tablets)

Dosage- 1-2 SALVICA-OZ Tablets once daily or in two divided doses.

Mode of Action-

Cefixime binds to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall, causing the inhibition of the third and last stage of bacterial cell wall synthesis. Cell lysis is then mediated by bacterial cell wall autolytic enzymes such as autolysins; it is possible that cefixime interferes with an autolysin inhibitor.

Ornidazole has selective toxicity to anaerobic microbes, the mechanism steps involves: Drug enters the cell by diffusion; nitro group of drug is reduced by redox proteins present only in anaerobic organisms to reactive nitro radical which exerts cytotoxic action by damaging DNA and other critical biomolecules; DNA helix destabilization and strand breakage has been observed.

Approx. Rs 350 / Piece Get Latest Price

We Salveo Lifecare, are one of the prominent suppliers of a wide range of Ceftazadime with Tazobactum injection. Our wide range includes Capsule, Soft gels, Tablets and Syrups. These are acknowledged for salient features such as purity, environment friendly and accurate composition. We welcome Qualified and experienced individuals as well as Corporates from Maharashtra to become our associates through PCD / Franchise. We offer to them good quality medicines at the most competitive rates in India.

Specifications:
• Type - Ceftazadime with Tazobactum
• Form - Injection
• Packaging - 1125 mg.
• Brand - Prozed-T We are looking for franchisee of our products in GHAZIPUR in Uttar Pradesh.