Lasix
- Product NDC
- 70518-2030
- 11-digit product format
- 705182030
- Labeler code
- 70518
- Product ID
- 70518-2030_86d4bb01-06bf-1d0b-e053-2a91aa0ada9c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FUROSEMIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA016273
- Marketing category
- NDA
- Marketing start
- 2019-04-18
- Marketing end
- 0000-00-00
- Substance
- FUROSEMIDE
- Active strength
- 20 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