Generated: September 21, 2017
DrugPatentWatch Database Preview
Details for New Drug Application (NDA): 018507
, which is a drug marketed by Sun Pharm Inds, Fresenius Kabi Usa, Watson Labs, Abraxis Pharm, Ipca Labs Ltd, Ivax Sub Teva Pharms, Astrazeneca, Dava Pharms Inc, Accord Hlthcare, Marsam Pharms Llc, Warner Chilcott, Smith And Nephew, West-ward Pharms Int, Intl Medication, Emcure Pharms Ltd, Watson Labs Teva, Hospira, Wockhardt, Baxter Hlthcare Corp, Sandoz, Amneal Pharms Co, Sun Pharm Inds Inc, Kalapharm, Wyeth Ayerst, Superpharm, Luitpold, Mylan, Mutual Pharm, Leading Pharma Llc, Igi Labs Inc, and Prinston Inc, and is included in fifty-seven NDAs. It is available from sixty-one suppliers. Additional details are available on the FUROSEMIDE profile page.
The generic ingredient in FUROSEMIDE is furosemide. There are twenty-one drug master file entries for this compound. Sixty-three suppliers are listed for this compound. Additional details are available on the furosemide profile page.
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Summary for product number 001
|Approval Date:||Jul 30, 1982||TE:||RLD:||No|
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