Furosemide
- Product NDC
- 55154-5477
- 11-digit product format
- 551545477
- Labeler code
- 55154
- Product ID
- 55154-5477_e83b3b98-f294-4a6f-8a52-f473da7e0323
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA070082
- Marketing category
- ANDA
- Marketing start
- 2010-10-12
- Marketing end
- 2019-05-31
- Substance
- FUROSEMIDE
- Active strength
- 80 mg/1
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record