Finasteride
- Product NDC
- 50090-2160
- 11-digit product format
- 500902160
- Labeler code
- 50090
- Product ID
- 50090-2160_9b7c629c-b114-45a5-bd87-53cb49679981
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090060
- Marketing category
- ANDA
- Marketing start
- 2013-07-01
- Marketing end
- 0000-00-00
- Substance
- FINASTERIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record