Bumetanide
- Product NDC
- 70518-1991
- 11-digit product format
- 705181991
- Labeler code
- 70518
- Product ID
- 70518-1991_854231e7-b2af-3229-e053-2a91aa0a7da1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074700
- Marketing category
- ANDA
- Marketing start
- 2019-03-28
- 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