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Serving leading biopharmaceutical companies globally:

Baxter
Cipla
Covington
Boehringer Ingelheim
Medtronic
Cantor Fitzgerald
Fish and Richardson
Chubb
Federal Trade Commission
Express Scripts

Generated: January 19, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 074332

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NDA 074332 describes BUMETANIDE, which is a drug marketed by Athenex Inc, Hospira, Teva Parenteral, West-ward Pharms Int, Amneal Pharms Co, Ivax Sub Teva Pharms, and Sandoz, and is included in eight NDAs. It is available from eighteen suppliers. Additional details are available on the BUMETANIDE profile page.

The generic ingredient in BUMETANIDE is bumetanide. There are five drug master file entries for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the bumetanide profile page.
Summary for 074332
Tradename:BUMETANIDE
Applicant:Hospira
Ingredient:bumetanide
Patents:0
Therapeutic Class:Cardiovascular Agents
Formulation / Manufacturing:see details
Pharmacology for NDA: 074332
Medical Subject Heading (MeSH) Categories for 074332
Suppliers and Packaging for NDA: 074332
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
BUMETANIDE bumetanide INJECTABLE;INJECTION 074332 ANDA Hospira, Inc. 0409-1412 0409-1412-04 10 VIAL in 1 BOX (0409-1412-04) > 4 mL in 1 VIAL
BUMETANIDE bumetanide INJECTABLE;INJECTION 074332 ANDA Hospira, Inc. 0409-1412 0409-1412-10 10 VIAL, MULTI-DOSE in 1 BOX (0409-1412-10) > 10 mL in 1 VIAL, MULTI-DOSE

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrength0.25MG/ML
Approval Date:Oct 31, 1994TE:APRLD:No

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Serving leading biopharmaceutical companies globally:

Johnson and Johnson
US Department of Justice
Dow
Mallinckrodt
Argus Health
US Army
Harvard Business School
Farmers Insurance
QuintilesIMS

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