Bumetanide
- Product NDC
- 68071-2019
- 11-digit product format
- 680712019
- Labeler code
- 68071
- Product ID
- 68071-2019_3b64e7dd-d0cf-4be0-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA074225
- Marketing category
- ANDA
- Marketing start
- 2007-10-16
- Marketing end
- 0000-00-00
- Substance
- BUMETANIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Loop Diuretic [EPC],Increased Diuresis at Loop of Henle [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record