Salveo Lifecare
Salveo Lifecare
Dhakoli, Mohali, Punjab
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Salveois a Latin word that means "to be well" or“being healthy”. This is indicative of the vision of the company, it’s the commitment to provide cure from the sufferings of the mankind by providing allopathic products of international quality at an affordable price. Our logo, a rising sun symbolizes the birth of a new pharma company that will provide service in the field of healthcare. The rising sun also represents the fact that, as a company, we will provide the necessary energy, seek the best from different sources, and integrate them under theSalveobrand, keep evolving and growing.

Salveo Lifecarecame into existence in 2008 with the objective of profitably marketing allopathic medicines through direct marketing of its products and through its channel partners. The company has its operational office at Zirakpur and is managed by a group of professionals having experience of handling pharma business for more than 30 years. The products ofSalveo Lifecareare well established molecules in the various therapeutic segments viz.Anti-infectives, Anti-Ulcerants, Pain management-Analgesics/Anti rheumatics/anti-inflammatory, Nutritional and health supplements, Anti-oxidants/Multi-vitamins, Anti-asthmatics, Cough management, Haematinics, Anti-allergics, Digestive enzyme, Anti-osteoporotic, Prebiotics-Probiotics sachets and capsules, Ear-drops, Neuro-protectives, Hepato-protectives, Anti-diabetics, Cardiac care, Neuro-Psychiatry, Cardiac care.???

Salveo Lifecareis the main flagship company and has other divisions namelyNuphoric Lifesciences and Progenica Biopharma. The products of Salveo Lifecare and its divisions have been thoroughly tested on various parameters and manufactured atGoodManufacturing Practices (GMP)/ISO 9001:2000/ ISO 9001:2008 certified units.

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Product Details:
Minimum Order Quantity100 Strip
Dose/Strength (ex. 1 mg or 1ml)AS ADVISED BY PHYSICIAN
Packaging TypeALU ALU STRIP
UsageClinical
Packaging Size10x10

Olmifab-H Tablets

Olmesartan       20 mg

Hydrochlorthiazide 12.5 mg

 

Uses
Olmesartan is used to treat high blood pressure (hypertension), prevention and treatment of heart attack (Myocardial Infarction) and heart failure; when heart is unable to pump sufficient blood. It is also used in patients of diabetes with kidney failure.

Hydrochlorothiazide is used to treat high blood pressure (hypertension). It also treats fluid retention (edema) due to congestive heart failure or cirrhosis of liver or kidney disorder.

How it works

Olmesartan belongs to a class of medications called angiotensin II receptor inhibitors. Angiotensin II is a chemical that causes muscles surrounding the blood vessels to contract, thereby narrowing the blood vessels. Olmesartan is an angiotensin II receptor blocker (ARB) resulting in relaxation of blood vessels, and thus, reduces blood pressure.

 

Hydrochlorothiazide belongs to class of medications called thiazide diuretics. It acts by eliminating the fluid and salts from the body. It works on the kidneys to produce more urine which removes extra water and certain salts from the body which in turn lowers blood pressure and swelling.

Olmesartan and Hydrochlorthiazide when given together, help to lower blood pressure more than if either of them were given alone.

Dose
The recommended starting dose of Olmifab-H is 20/12.5 mg once daily in patients whose blood pressure is not adequately controlled with HCT monotherapy or who experience dose-limiting adverse reactions with hydrochlorothiazide. Dose can be titrated up to 40 /25 mg if necessary.   Indications

Hypertension not controlled with Olmesartan alone.

  Contra Indications Anuria, severe renal and hepatic failure, hypersensitivity, refractory hypokalaemia and hyponatraemia, hypercalaemia and symptomatic hyperuricaemia. Sulphonamide allergy. Pregnancy and lactation

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Dosage FormTablet
Form Of MedicineTablets
Packaging Size1x10
Packaging TypeAluminium-Aluminium

FENASAL-SR

Each Hard Gelatin Capsule Contains:

Aceclofenac IP (As Sustained Release) 200 mg

Rabeprazole Sodium IP (As Enteric Coated) 20 mg

Aceclofenac & Rabeprazole Capsule

We are marketing combination of Aceclofenac and Rabeprazole and we know that Aceclofenac belongs to the group of anti-inflammatory drugs used for the treatment of inflammatory and painful such as low back pain, toothache and joint pain, osteoarthritis and rheumatoid arthritis.

 

Rabeprazole Sodium is an antiulcer drug in the class of proton pump inhibitors. Proton pump inhibitors act by irreversibly blocking the hydrogen/potassium adenosine triphosphatase enzyme system (the H+/K+ ATPase, or more commonly, the gastric proton pump) of the gastric parietal cells. The proton pump is the terminal stage in gastric acid secretion, being directly responsible for secreting H+ ions into the gastric lumen, making it an ideal target for inhibiting acid secretion.

 

Indication and Usage:

● Treatment of duodenal ulcers

● Gastroesophageal reflux disease (GERD)

● Maintaining healing and reducing relapse rates of heartburn symptoms in patients with GERD

● Peptic ulcer disease (PUD)

● Treatment of pathological hypersecretory conditions (Zollinger-Ellison syndrome)

Mechanism of Action:

Combination of Aceclofenac and Rab eprazole is very effective against mild to moderate pain and ulcers. Like other NSAIDS, it has anti-inflammatory and analgesic activity and work by inhibiting the action of synthesis through the inhibition of both COX-1 and COX-2. This leads to the reduction of inflammation, pain, fever, and swelling, which are mediated by prostaglandins.

 

Rabeprazole belongs to a class of antisecretory compounds (substituted benzimidazole proton-pump inhibitors) that do not exhibit anticholinergic or histamine H2-receptor antagonist properties, but suppress gastric acid secretion by inhibiting the gastric H+, K+ATPase at the secretory surface of the gastric parietal cell. Because this enzyme is regarded as the acid (proton) pump within the parietal cell, rabeprazole has been characterized as a gastric proton-pump inhibitor. Rabeprazole blocks the final step of gastric acid secretion.

 

Drug Interactions:

BEFORE TAKING THIS TELL THE DOCTOR ABOUT ANY MEDICAL PROBLEMS AN ALLERGIES THAT PATIENT HAS NOW OR HAS HAD.

Usually drug interactions occur when it is taken with another drug or with food. Before you take a medication for a particular ailment, you should inform the health expert about intake of any other medications including non-prescription medications. Aceclofenac and Rabeprazole may increase plasma concentrations of lithium, digoxin and methotrexate, increase the activity of anticoagulant, inhibits the activity of diuretics, enhance cyclosporin nephrotoxicity and precipitate convulsions when co-administered with quinolone antibiotics. And also decreases the concentration of ketoconazole in the plasma (in 33%), increases the concentration of digoxin (in 22%), and does not interact with liquid antacids.

 

Adverse Effects:

Headache, abdominal pain, dry mouth, dizziness, nausea and diarrhea.

 

Conclusion:

We are marketing Combination of Aceclofenac and rabeprazole which is superior form other NSAIDs as it has selectivity for cox-2, a beneficial cox inhibitor, well tolerated, better GI tolerability and improved cardiovascular safety when compared to other selective cox-2 inhibitors with combination of rabeprazole it work as gastric proton-pump inhibitor. It also work against Gastroesophageal reflux disease by blocking the final step of gastric acid secretion by inhibiting the gastric H+, K+ATPase at the secretory surface of the gastric parietal cell.



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FormTablets
Packing TypeBox

Description

  • disclaimer the information given below is for the use of medical sales rep and is not for doctors. Information given below is inadequate for treating a patient

garitel-40 tablet

composition

telmisartan ip 40 mg

telmisartan is a newer type of blood pressure medicine known as an angiotensin ii receptor blocker (arb for short). As the name implies, telmisartan blocks angiotensin ii receptors. This decreases the effectiveness of a chemical known as angiotensin ii, which normally causes blood vessels to narrow (constrict). By blocking the effects of angiotensin ii, telmisartan causes blood vessels to relax.

indications and usage

high blood pressure (hypertension)

drug interaction

Complementry mechanism of action

Reduction in peripheral resistence with arb

Reduction of fluid volume with diuretics

Arbs counteract reactive increase in blood pressure related to diuretic induced renin secretion

Arbs ameliorates diuretic induced potassium depletion

Well tolerated; fewer metabolic disturbances

No significant variation in pharmacokinetic parameters of telmisartan in presence of hydrochloroth.iazide

combination of telmisartan with hydrochlorot.hiazide was found to be more effective than each agent alone in lowering blood pressure. Indeed , combining telmisartan with hydrochlorothia.zide enhances the antihypertensive efficacy of telmisartan in patients not adequately controlled with telmisartan alone.

pharmacokinetic

telmisartan is orally well absorbed and metabolized to an active metabolite which is more potent than losartan as at1 antagonist. Orally administered hydrochlor.othiazide is rapidly absorbed and diuretic effect is seen in 1 hour and their duration lasts up to 12-24 hours. Both telmisartan and hydroc.hlorothiazide has longer duration of actions. These agents are bound to plasma proteins to varying degrees and this has no correlation to their half-life.

pharmacodynamics

the pharmacodynamics of telmisartan & hydrochlo.rothiazide has been investigated in vitro and in vivo in rodents, guinea pigs, rabbits and dogs. The combination of telmisartan with hydroc.hlorothiazide (40 mg/12. 5 mg and 80 mg/12. 5 mg) is expected to benefit patients with hypertension who are not adequately responsive to telmisartan alone.

contraindications

Second and third trimesters of pregnancy.

Biliary obstructive disorders.

Severe hepatic impairment.

storage

this medicinal product does not require any special temperature storage conditions. Store in the original package in order to protect from moisture.


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Packaging TypeBox
UsageHospital, Clinical

Telmisartan And Amlodipine (Oral Route) Descriptions

Telmisartan and amlodipine is a combination of medicines that may be used alone or with other medicines to treat high blood pressure (hypertension). High blood pressure adds to the workload of the heart and arteries. If it continues for a long time, the heart and arteries may not function properly. This can damage the blood vessels of the brain, heart, and kidneys, resulting in a stroke, heart failure, or kidney failure. Lowering blood pressure can reduce the risk of strokes and heart attacks.

Telmisartan is an angiotensin II receptor blocker (ARB). It works by blocking a substance in the body that causes blood vessels to tighten. As a result, the blood vessels relax and this decreases blood pressure. When blood pressure is lowered, the amount of blood and oxygen that go to the heart is increased.

Amlodipine is a calcium channel blocker (CCB). It affects the movement of calcium into the cells of the heart and blood vessels. As a result, amlodipine relaxes the blood vessels and increases the supply of blood and oxygen to the heart while reducing its workload.

This medicine is available only with your doctor's prescription.

This product is available in the following dosage forms:

· Tablet


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UsageClinical

Depisal-a tablet

Each tablet contains

Atenolol 50 mg

Amlodipine 5 mg

Atenolol is a cardioselective beta blocker.
Amlodipine is a dihydropyridine calcium channel blocker that blocks the transmembrane influx of calcium ions into vascular smooth muscle and cardiac muscle.

Pharmacokinetics

Combination of the two drugs results in additive antihypertensive action.

Absorption:

Amlodipine: Plasma levels peak 6-12 hr after oral admin; absolute bioavailability is estimated to be 64-90%.

Atenolol:

Absorption is rapid and consistent but incomplete; about 50% of an oral dose is absorbed in the GI tract; plasma levels peak 2-4 hr after oral admin.

Distribution:

Amlodipine: 93% bound to plasma proteins.

Atenolol: 6-16% bound to plasma proteins.

Metabolism:

Amlodipine: About 90% converted to inactive metabolites hepatically.

Atenolol: Little or no hepatic metabolism.

Excretion:

Amlodipine: 10% of parent compound and 60% of the metabolites are removed in the urine; elimination from the plasma is biphasic with terminal half-life of about 30-50 hr. Atenolol: 50% of the oral dose is removed unchanged in the faeces; absorbed drug is removed mainly via renal elimination; half-life is about 6-7 hr.

 

Atenolol + Amlodipine Indications / Atenolol + Amlodipine Uses

Antihypertensive activity

Atenolol + Amlodipine Adverse Reactions / Atenolol + Amlodipine Side Effects

Headache, hypotension, dizziness, breathlessness, fatigue, muscle cramps, bradycardia, palpitations, flushing, oedema, dyspnoea, dyspepsia, cold extremities. Drowsiness, chestpain impotence rarely. Hypersensitivity reactions.

Precautions

Overdosage may cause hypotension and less commonly, congestive cardiac failure. Unabsorbed drug may be removed by gastric lavage or use of activated charcoal. Symptomatic treatment may be administered.

 

Special Precautions

Excessive fall of BP may occur in elderly patients. Caution in patients with COPD, thyrotoxicosis, congestive failure, vasospastic angina, hepatic renal impairment. Caution in diabetic patients as beta-blockers may mask tachycardia occurring with hypoglycaemia. Withdrawal should be gradual. Lactation. Safety and efficacy have not been established in children. Not to be used in untreated phaeochromocytoma.

 

 

Other Drug Interactions

Additive effect when used with catecholamine depleting drugs; monitor for hypotension and/or marked bradycardia. If used with clonidine, clonidine withdrawal should occur a few days after withdrawal of the beta-blocker to prevent rebound hypertension; if replacing clonidine by beta-blocker, beta-blocker should be introduced only after clonidine administration has stopped for several days. Concurrent use with prostaglandin synthase inhibiting drugs (e.g. indomethacin) may reduce the hypotensive effects of beta-blockers.

 

Dosage

Oral
Chronic stable angina, Hypertension

Adult: Per tablet contains atenolol 25 or 50 mg and amlodipine (as besylate) 5 mg: 1 tab once daily, may increase to 2 tablets daily if needed. 

Elderly: Per tablet contains atenolol 25 mg and amlodipine (besylate) 5 mg: Initiate with 1 tablet daily. 

Renal impairment: Per tablet contains atenolol 25 mg and amlodipine (besylate) 5 mg: Initiate with 1 tablet daily.



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Metformin SR 500 mg,
Pioglitazone 15 mg
Glimepiride 2 mg

J Indian Med Assoc. 2005 Aug;103(8):447-50.Evaluation of efficacy and safety of fixed dose combination of glimepiride 2 mg pluspioglitazone 15 mg plus metformin SR 500 mg in the management of patients with type-2 diabetes mellitus.Meshram DM1, Langade DG, Kinagi SB, Naikwadi AA, Morye V, Chopra D AbstractAn estimated 25 million Indians currently have diabetes and the projections indicate Indians would be the largest group by the year 2025 AD. An open, phase III, multicentric study was conducted to determine the efficacy and tolerability of the triple drug combination glimepiride 2 mg plus pioglitazone hydrochloride 15 mg plus metformin SR 500 mg for 8 weeks in 101 Indian patients with type 2 diabetes mellitus. The study revealed that the triple drug combination could achieve the recommended goals, recommended by American Diabetic Association, for fasting blood glucose < or = 140 mg/dl and glycosylated haemoglobin (HbA1c) of < or = 8%. After 8 weeks, the mean fasting blood glucose (baseline 189.61) was reduced to 111.68 (41% reduction); the mean glycosylated haemoglobin (baseline 10.32) was significantly reduced to 7.54 (26% reduction). The triple drug combination significantly reduced the levels of triglyceride, low density lipoproteins and total cholesterol. These significant levels were achieved within 8 weeks and all patients tolerated the drug well with no reported case of serious adverse events including hypoglycaemia. There were also no reported drug interactions in the study. Since the decrease in HbA1c was continuous and throughout the study, a further decrease in the HbA1c levels would have been noted since the present trial was designed for a period of 8 weeks. Thus, the present study confirms the efficacy and safety of FDC of the triple drug combination in patients with type 2 diabetes.

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Product Details:
Minimum Order Quantity100 Strip
Packaging TypeBox
UsageHospital, Clinical
Packaging Size10x10 Tablets

We are highly appreciated by the clients for manufacturing and supplying Cardio Diabetic Drugs. Moreover, the plates offered by us are tested on various parameters so as to ensure their high purity. Tested as per the international standards of quality, these products are in high demand in the market.

Features:

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

Uses:

  • Glykad 62 Tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.

Specification:

  • Composition: Metformin 1000 mg, Glimipride 2 mg.

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.



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    • Item Code: Glykad-Tablets

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    Product Details:
    Packaging10x10 tablets
    Packaging TypeStrips, Box
    Product TypeAllopathic

    We are into a business of Pharma Franchise,Pharma PCD range of Pharma Medicines that are incompliance with the WHO-GMP standards & safe toconsume & give the aid from suffering from variousdiseases.

    We are making our name in offering the nation with a series of affordable and innovative medicines for a healthier living, for all. We are here presenting a range of Pharma PCD, Pharma Franchise, Pharmaceutical Capsules, Pharmaceutical Tablets, Soft Gel Capsules, Pharmaceutical Syrups, Dry Syrups, Pharmaceutical Injections and Pharmaceutical Drops.

    As an integrated healthcare solutions provider, we cater to several therapeutic areas. We have also established a cordial relations with reliable vendors from whom we procure the range. Moreover, our agents, Pharma Franchise, Pharma PCD ensure that these are processed using quality ingredients and advanced manufacturing techniques. Our pharmaceutical products are quality tested on different parameters to ensure these are in compliance with the WHO-GMP standards. All our medicines are highly effective and do not have any side effects.

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

    "Third party inquiries are also solicited"

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    Product Details:
    Minimum Order Quantity100 Strip
    Packaging Size10
    Packaging TypeSTRIP
    UsageHospital

    Garitel-H Tab

    Each tablet contains

    Telmisartan IP 40 mg

    Hydrochlorthiazide IP 12.5 mg

    Telmisartan is a newer type of blood pressure medicine known as an angiotensin II receptor blocker (ARB for short). As the name implies, telmisartan blocks angiotensin II receptors. This decreases the effectiveness of a chemical known as angiotensin II, which normally causes blood vessels to narrow (constrict). By blocking the effects of angiotensin II, telmisartan causes blood vessels to relax.

    Hydrochlorothiazide is a diuretic, which is commonly referred to as a "water pill." It works by increasing the amount of salt and water that the kidneys remove from the blood. This extra salt and water are passed out through the urine. By increasing the amount of water removed from the blood, hydrochlorothiazide causes a decrease in blood volume.

    Indications and Usage
    High Blood Pressure (Hypertension)

    Drug Interaction
    Complementry mechanism of action
    Reduction in peripheral resistence with ARB
    Reduction of fluid volume with Diuretics
    ARBs counteract reactive increase in blood pressure related to diuretic induced renin secretion
    ARBs ameliorates diuretic induced potassium depletion
    Well tolerated; fewer metabolic disturbances
    No significant variation in pharmacokinetic parameters of telmisartan in presence of hydrochlorothiazide
    Combination of telmisartan with hydrochlorothiazide was found to be more effective than each agent alone in lowering blood pressure. Indeed , combining telmisartan with hydrochlorothiazide enhances the antihypertensive efficacy of telmisartan in patients not adequately controlled with telmisartan alone.

    Pharmacokinetic
    Telmisartan is orally well absorbed and metabolized to an active metabolite which is more potent than Losartan as AT1 antagonist. Orally administered hydrochlorothiazide is rapidly absorbed and diuretic effect is seen in 1 hour and their duration lasts up to 12-24 hours. Both telmisartan and hydrochlorothiazide has longer duration of actions. These agents are bound to plasma proteins to varying degrees and this has no correlation to their half-life.

    Pharmacodynamics
    The pharmacodynamics of telmisartan hydrochlorothiazide has been investigated in vitro and in vivo in rodents, guinea pigs, rabbits and dogs. The combination of telmisartan with hydrochlorothiazide (40 mg/12.5 mg and 80 mg/12.5 mg) is expected to benefit patients with hypertension who are not adequately responsive to telmisartan alone.

    Contraindications
    Second and third trimesters of pregnancy.
    Biliary obstructive disorders.
    Severe hepatic impairment.

    Conclusion
    This is a new combination for a muscle relaxant and displays anti - inflammatory and analgesic properties. Thiocolchicoside Diclofenac Sodium is well absorbed from the gastrointestinal tract. It shows its effect in 1 - 2 hr after oral administration. This combination is used to treat various painful inflammatory conditions. Diclofenac Sodium has an outstanding anti-inflammatory profile mediated primarily through inhibition of cyclooxygenase (COX) activity and suppression of PGE2 synthesis From the above discussion, it can be concluded that this medicine could improve the quality of life of patients with as well as muscle relaxant in addition. Moreover it has a considerable safety profile, with persistent results.

    Storage
    This medicinal product does not require any special temperature storage conditions. Store in the original package in order to protect from moisture.v

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    Salveo Lifecare
    Tarandeep Singh Vohra  (Sales Manager)
    SCO-6, Guru Gobind Singh Nagar Dhakoli
    Mohali - 140603 , Punjab , India
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