Furosemide
- Product NDC
- 50090-2187
- 11-digit product format
- 500902187
- Labeler code
- 50090
- Product ID
- 50090-2187_5dd52ff1-deca-48a0-a859-ac1a3920ee6a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA070082
- Marketing category
- ANDA
- Marketing start
- 1986-10-29
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record