Furosemide
- Product NDC
- 70518-1072
- 11-digit product format
- 705181072
- Labeler code
- 70518
- Product ID
- 70518-1072_90110704-15a3-6478-e053-2995a90a6b65
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA018487
- Marketing category
- NDA
- Marketing start
- 2018-03-19
- Marketing end
- 0000-00-00
- Substance
- FUROSEMIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record