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Last Updated: January 29, 2022

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 074700


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NDA 074700 describes BUMETANIDE, which is a drug marketed by Athenex Inc, Hospira, Teva Parenteral, West-ward Pharms Int, Amneal Pharms Co, Heritage Pharma, Rising, Sandoz, Upsher Smith Labs, and Zydus Pharms, and is included in eleven NDAs. It is available from nineteen suppliers. Additional details are available on the BUMETANIDE profile page.

The generic ingredient in BUMETANIDE is bumetanide. There are six drug master file entries for this compound. Twenty-four suppliers are listed for this compound. Additional details are available on the bumetanide profile page.
Summary for 074700
Tradename:BUMETANIDE
Applicant:Sandoz
Ingredient:bumetanide
Patents:0
Formulation / Manufacturing:see details
Pharmacology for NDA: 074700
Medical Subject Heading (MeSH) Categories for 074700
Suppliers and Packaging for NDA: 074700
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
BUMETANIDE bumetanide TABLET;ORAL 074700 ANDA Eon Labs, Inc. 0185-0128 0185-0128-01 100 TABLET in 1 BOTTLE (0185-0128-01)
BUMETANIDE bumetanide TABLET;ORAL 074700 ANDA Eon Labs, Inc. 0185-0128 0185-0128-05 500 TABLET in 1 BOTTLE (0185-0128-05)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength0.5MG
Approval Date:Nov 21, 1996TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength1MG
Approval Date:Nov 21, 1996TE:ABRLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength2MG
Approval Date:Nov 21, 1996TE:ABRLD:No

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