Finasteride
- Product NDC
- 71713-099
- 11-digit product format
- 717130099
- Labeler code
- 71713
- Product ID
- 71713-099_3fe7bdaa-b027-4da9-94ee-550bf28c63e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Finasteride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Thirty Madison Inc
- Application
- ANDA207750
- Marketing category
- ANDA
- Marketing start
- 2021-03-22
- 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 |
|---|
| 71713-099-90 | Finasteride | 90 in 1 CONTAINER | TABLET | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71713-099 | FINASTERIDE TABLET [THIRTY MADISON INC] | 1 | Current NDC, Legacy NDC, 1 package rows | 20210413_3fe7bdaa-b027-4da9-94ee-550bf28c63e1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71713-099-90 | 71713009990 | 90 TABLET in 1 CONTAINER (71713-099-90) | 90 tablet | 2021-03-22 | 0000-00-00 | No | No | Current |