Finasteride
- Product NDC
- 68071-3744
- 11-digit product format
- 680713744
- Labeler code
- 68071
- Product ID
- 68071-3744_2a091864-3ec9-044f-e063-6294a90adc98
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Finasteride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA207750
- Marketing category
- ANDA
- Marketing start
- 2017-01-06
- 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
- 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 | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 57GNO57U7G |
| Rxcui | 200172 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-3744-6 | Finasteride | 60 in 1 BOTTLE | TABLET, COATED | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-3744 | FINASTERIDE TABLET, COATED [NUCARE PHARMACEUTICALS, INC.] | 2 | Current NDC, 1 package rows | 20241226_291a2037-2b4f-a2fe-e063-6294a90a1e9a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3744-6 | 68071374406 | 60 TABLET, COATED in 1 BOTTLE (68071-3744-6) | 2024-12-12 | No | No | Current |