Finasteride
- Product NDC
- 55154-2639
- 11-digit product format
- 551542639
- Labeler code
- 55154
- Product ID
- 55154-2639_fb0070db-2941-43c3-91d4-f028ea28e097
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA090061
- Marketing category
- ANDA
- Marketing start
- 2025-02-10
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Finasteride
- Listing expiration
- 2027-12-31
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 |
|---|
| 55154-2639-0 | Finasteride | 10 in 1 BAG | TABLET, FILM COATED | 10 | | 3 |
| 55154-2639-0 | Finasteride | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55154-2639 | FINASTERIDE TABLET, FILM COATED [CARDINAL HEALTH 107, LLC] | 1 | Current NDC, 2 package rows | 20250212_22161236-6804-4a7f-86cb-cfa20bd1951e.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 |
|---|
| 55154-2639-0 | 55154263900 | 10 BLISTER PACK in 1 BAG (55154-2639-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2025-02-10 | No | No | Current |