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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Finasteride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FINASTERIDE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 57GNO57U7G |
| Rxcui | 310346 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7228-0 | Finasteride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
| 50090-7228-0 | Finasteride | 12 in 1 CASE | TABLET, FILM COATED | 12 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7228 | FINASTERIDE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 1 | Current NDC, 2 package rows | 20240827_d66fe4bd-534b-4674-a346-0cf3cdabbfaa.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |