Finasteride
- Product NDC
- 50090-7228
- 11-digit product format
- 500907228
- Labeler code
- 50090
- Product ID
- 50090-7228_d2c13767-15d7-436c-84c2-3fa74af1c63d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090061
- Marketing category
- ANDA
- Marketing start
- 2015-06-13
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 57GNO57U7G | FINASTERIDE | 98319-26-7 | FINASTERIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7228-0 | 50090722800 | 12 BOTTLE in 1 CASE (50090-7228-0) / 30 TABLET, FILM COATED in 1 BOTTLE | 12 bottle | 2024-08-22 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Finasteride | A-S Medication Solutions | 2024-08-26 | Human Prescription Drug Label | 1 |