Famotidine (Famotidine)

Trade Name : Famotidine

Bryant Ranch Prepack

TABLET, FILM COATED

Strength 20 mg/1

FAMOTIDINE Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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You can fill in a request for your medicine through the form provided. You can access the form by clicking on the ‘Get Price’ button.

Product information is meant for

Wholesalers Suppliers Exporters Doctors MOH Tender Supplies Hospitals Brand CROs Comparator Supplies Generic Cooperate Sourcing Individual Patients Indian Institutional Buyers

Disclaimer

Trade Marks displayed in compliance with provisions of: Trademark Act, 1999 u/s 30 and 30 (1) of "Fair use"

GNH India is WHO GDP and ISO 9001 2015 Certified Pharmaceutical Wholesaler/ Supplier/ Exporters/ Importer from India of Famotidine (Famotidine) which is also known as Famotidine and Manufactured by Bryant Ranch Prepack. It is available in strength of 20 mg/1 per ml. Read more

Famotidine (Famotidine) is supplied for Tenders/ Emergency imports/ Un - licensed, Specials, Orphan drug/ Name patient line/ RLD supplies/ Reference listed drugs/ Comparator Drug/ Bio-Similar/ Innovator samples For Clinical trials.  Click to know price.     Read less

Packaging and Delivery

Validated Cold Chain Shipment

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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About GNH

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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  • No data
  • Famotidine tablets are indicated in adult and pediatric patients 40 kg andu00a0greater for the treatment of:
  • Famotidine tablets are indicated in adults for the:
  • Famotidine is a histamine-2 (H) receptor antagonist indicated :
  • In adult and pediatric patients 40 kg and greater for the treatment of:
  • u00a0In adults for the:
  • u00a0n :
  • u00a0
  • Tablets: 20 mg, 40 mg n
  • Famotidine tablets are contraindicated in patients with a history of serious hypersensitivity reactions (e.g., anaphylaxis) to famotidine or otheru00a0histamine-2 (H) receptor antagonists.
  • History of serious hypersensitivity reactions (e.g., anaphylaxis) to famotidine or other H receptor antagonists. n
  • No data
  • Central Nervous System (CNS) Adverse Reactions
  • GI Malignancy
  • The most common adverse reactions are: headache, dizziness, constipation, and diarrhea. n
  • To report SUSPECTED ADVERSE REACTIONS, contact Aurobindo Pharma USA, Inc. at 1-866-850-2876 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
  • No data
  • Drugs Dependent on Gastric pH for Absorption
  • Tizanidine (CYP1A2) Substrate:
  • No data
  • Geriatric Use:
  • Renal Impairment:
  • The types of adverse reactions in overdosage of famotidine are similar to the adverse reactions encountered with use of recommended dosages .
  • In the event of overdosage, treatment should be symptomatic and supportive. Unabsorbed material should be removed from the gastrointestinal tract, the patient should be monitored, and supportive therapy should be employed.
  • Due to low binding to plasma proteins, famotidine is eliminated by hemodialysis. There is limited experience on the usefulness of hemodialysis as a treatment for famotidine overdosage.
  • The active ingredient in famotidine tablets USP is a histamine-2 (H) receptor antagonist. Famotidine is u00a0u2032u00ad(aminosulfonyl)-3-[[[2-[(diaminomethylene)amino]-4-thiazolyl]methyl]thio] propanimidamide. The molecular formula of famotidine is CHNOS and its molecular weight is 337.43. Its structural formula is:
  • Each famotidine tablet for oral administration contains either 20 mg or 40 mg of famotidine USP and the following inactive ingredients: carnauba wax, corn starch, hydroxypropyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, sodium starch glycolate, talc, and titanium dioxide. In addition the 20 mg tablets contain red iron oxide, and yellow iron oxide.
  • Famotidine USP is a white to pale yellowish white crystalline powder that is freelyu00a0soluble in glacial acetic acid, slightly soluble in methanol, very slightly u00a0soluble in water, and practically insoluble in ethanol.
  • No data
  • Carcinogenic potential of famotidine was assessed in a 106-week oral carcinogenicity study in rats and a 92-week oral carcinogenicity study in mice. In the 106-week study in rats and the 92-week study in mice at oral doses of up to 2000 mg/kg/day (approximately 243 and 122 times, respectively, based on body surface area, the recommended human dose of 80 mg per day for the treatment of erosive esophagitis), there was no evidence of carcinogenic potential for famotidine.
  • Famotidine was negative in the microbial mutagen test (Ames test) using and with or without rat liver enzyme activation at concentrations up to 10,000 mcg/plate. In studies in mice, with a micronucleus test and a chromosomal aberration test, no evidence of a mutagenic effect was observed.
  • In studies with rats given oral doses of up to 2000 mg/kg/day (approximately 243 times, based on body surface area, the recommended human dose of 80 mg per day) fertility and reproductive performance were not affected.
  • No data
  • Product: 71335-0370
  • NDC: 71335-0370-1 30 TABLET, FILM COATED in a BOTTLE
  • NDC: 71335-0370-2 60 TABLET, FILM COATED in a BOTTLE
  • NDC: 71335-0370-3 20 TABLET, FILM COATED in a BOTTLE
  • NDC: 71335-0370-4 90 TABLET, FILM COATED in a BOTTLE
  • NDC: 71335-0370-5 100 TABLET, FILM COATED in a BOTTLE
  • NDC: 71335-0370-6 10 TABLET, FILM COATED in a BOTTLE
  • NDC: 71335-0370-7 120 TABLET, FILM COATED in a BOTTLE
  • NDC: 71335-0370-8 50 TABLET, FILM COATED in a BOTTLE
  • Central Nervous System (CNS) Adverse Reactions n- [see ]
  • QT Prolongation n- [see ]
  • Administration
  • Advise patients:
  • Distributed by:n 279 Princeton-Hightstown Road East Windsor, NJ 08520n Manufactured by:n Hyderabadu2013500 038, Indian Revised: 05/2019
  • No data

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