Finasteride
- Product NDC
- 55700-508
- 11-digit product format
- 557000508
- Labeler code
- 55700
- Product ID
- 55700-508_63bba1f3-65d2-4069-93a4-2a4e2b579146
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA077578
- Marketing category
- ANDA
- Marketing start
- 2015-10-20
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record