FINASTERIDE
- Product NDC
- 63629-5220
- 11-digit product format
- 636295220
- Labeler code
- 63629
- Product ID
- 63629-5220_3d98793e-79cc-41e4-aebd-584c1a531457
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FINASTERIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078371
- Marketing category
- ANDA
- Marketing start
- 2013-11-05
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record