FUROSEMIDE
- Product NDC
- 60760-624
- 11-digit product format
- 607600624
- Labeler code
- 60760
- Product ID
- 60760-624_7b327707-642f-568f-e053-2a91aa0a112d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FUROSEMIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St Marys Medical Park Pharmacy
- Application
- ANDA078010
- Marketing category
- ANDA
- Marketing start
- 2013-05-09
- Marketing end
- 2019-09-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record