Finasteride
- Product NDC
- 68071-4044
- 11-digit product format
- 680714044
- Labeler code
- 68071
- Product ID
- 68071-4044_566a8fd7-fba8-2297-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA090121
- Marketing category
- ANDA
- Marketing start
- 2010-05-28
- Marketing end
- 0000-00-00
- Substance
- FINASTERIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record