Bumetanide
- Product NDC
- 68071-3023
- 11-digit product format
- 680713023
- Labeler code
- 68071
- Product ID
- 68071-3023_a4ed7a99-4d8e-a3f9-e053-2995a90abb98
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc..
- Application
- ANDA074700
- Marketing category
- ANDA
- Marketing start
- 1996-11-21
- Marketing end
- 2020-12-31
- Substance
- BUMETANIDE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Loop Diuretic [EPC],Increased Diuresis at Loop of Henle [PE]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record