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Serving leading biopharmaceutical companies globally:

Cerilliant
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US Department of Justice
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Generated: October 17, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 076796

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NDA 076796 describes FUROSEMIDE, 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-three 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-five suppliers are listed for this compound. Additional details are available on the furosemide profile page.

Summary for NDA: 076796

Tradename:
1
Applicant:
1
Ingredient:
1
Patents:0
Therapeutic Class:Cardiovascular Agents
Formulation / Manufacturing:see details

Pharmacology for NDA: 076796

Suppliers and Packaging for NDA: 076796

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
FUROSEMIDE
furosemide
TABLET;ORAL 076796 ANDA Qualitest Pharmaceuticals 0603-3739 0603-3739-21 100 TABLET in 1 BOTTLE, PLASTIC (0603-3739-21)
FUROSEMIDE
furosemide
TABLET;ORAL 076796 ANDA Qualitest Pharmaceuticals 0603-3739 0603-3739-32 1000 TABLET in 1 BOTTLE, PLASTIC (0603-3739-32)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength20MG
Approval Date:Mar 26, 2004TE:ABRLD:No

Summary for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength40MG
Approval Date:Mar 26, 2004TE:ABRLD:No

Summary for product number 003

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength80MG
Approval Date:Mar 26, 2004TE:ABRLD:No


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Serving leading biopharmaceutical companies globally:

McKesson
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McKinsey
Cerilliant

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