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Last Updated: December 12, 2025

Details for New Drug Application (NDA): 218746


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NDA 218746 describes BUMETANIDE, which is a drug marketed by Aspiro, Gland, Hospira, Lupin Ltd, MSN, Qilu Pharm Hainan, Sagent, Teva Parenteral, West-ward Pharms Int, Amneal Pharms Co, Appco, Heritage Pharma, Jubilant Generics, Mankind Pharma, Rising, Rubicon Research, Sandoz, Taro, Upsher Smith Labs, and Zydus Pharms, and is included in twenty-one NDAs. It is available from thirty-four 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. Thirty-nine suppliers are listed for this compound. Additional details are available on the bumetanide profile page.
Summary for 218746
Tradename:BUMETANIDE
Applicant:Aspiro
Ingredient:bumetanide
Patents:0
Pharmacology for NDA: 218746
Medical Subject Heading (MeSH) Categories for 218746
Suppliers and Packaging for NDA: 218746
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
BUMETANIDE bumetanide INJECTABLE;INJECTION 218746 ANDA Camber Pharmaceuticals, Inc. 31722-368 31722-368-32 10 VIAL, SINGLE-DOSE in 1 CARTON (31722-368-32) / 4 mL in 1 VIAL, SINGLE-DOSE (31722-368-31)
BUMETANIDE bumetanide INJECTABLE;INJECTION 218746 ANDA Camber Pharmaceuticals, Inc. 31722-369 31722-369-32 10 VIAL, MULTI-DOSE in 1 CARTON (31722-369-32) / 10 mL in 1 VIAL, MULTI-DOSE (31722-369-10)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrength0.25MG/ML
Approval Date:Feb 27, 2025TE:APRLD:No

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