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Serving leading biopharmaceutical companies globally:

Express Scripts
Chubb
Cipla
US Department of Justice
Chinese Patent Office
Accenture
McKinsey
Cerilliant
Queensland Health
Teva

Generated: January 22, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 075799

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NDA 075799 describes FAMOTIDINE, which is a drug marketed by Hi-tech Pharma Co, Lupin Ltd, Navinta Llc, Apotex Inc, Apothecon, Athenex Inc, Fresenius Kabi Usa, Hospira, Mylan Labs Ltd, West-ward Pharms Int, Novel Labs Inc, Perrigo, Actavis Elizabeth, Alembic Pharms Ltd, Apotex, Aurobindo Pharma Ltd, Carlsbad, Dr Reddys Labs Ltd, Ivax Sub Teva Pharms, Mylan, Mylan Pharms Inc, Perrigo R And D, Sandoz, Sun Pharm Inds Ltd, Sun Pharm Industries, Teva, Watson Labs, Wockhardt, Abbvie, and Baxter Hlthcare, and is included in sixty-one NDAs. It is available from one hundred and sixteen suppliers. Additional details are available on the FAMOTIDINE profile page.

The generic ingredient in FAMOTIDINE is calcium carbonate; famotidine; magnesium hydroxide. There are two hundred and seventy-two drug master file entries for this compound. Twenty-seven suppliers are listed for this compound. Additional details are available on the calcium carbonate; famotidine; magnesium hydroxide profile page.
Summary for 075799
Tradename:FAMOTIDINE
Applicant:West-ward Pharms Int
Ingredient:famotidine
Patents:0
Therapeutic Class:Gastrointestinal Agents
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 075799

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrength10MG/ML
Approval Date:Apr 30, 2002TE:RLD:No

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Serving leading biopharmaceutical companies globally:

Merck
Accenture
Daiichi Sankyo
Fish and Richardson
Teva
US Department of Justice
Fuji
Federal Trade Commission
Cantor Fitzgerald

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