Finasteride
- Product NDC
- 68788-9517
- 11-digit product format
- 687889517
- Labeler code
- 68788
- Product ID
- 68788-9517_8b867706-e53e-488e-9a7c-64912581ff36
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA076436
- Marketing category
- ANDA
- Marketing start
- 2013-02-06
- 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