Finasteride
- Product NDC
- 50436-0455
- 11-digit product format
- 504360455
- Labeler code
- 50436
- Product ID
- 50436-0455_64d363d9-3dc1-4166-b0fc-699eb12eaca7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Finasteride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA207750
- Marketing category
- ANDA
- Marketing start
- 2017-01-06
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-0455-1 | Finasteride | 30 in 1 BOTTLE | TABLET, COATED | 30 | | 2 |
| 50436-0455-3 | Finasteride | 90 in 1 BOTTLE | TABLET, COATED | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0455 | FINASTERIDE TABLET, COATED [UNIT DOSE SERVICES] | 2 | Legacy NDC, 2 package rows | 20190119_42c47e93-adad-47b5-8d5c-f0f3e26e7444.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0455-1 | 50436045501 | 30 in 1 BOTTLE | Historical |
| 50436-0455-3 | 50436045503 | 90 in 1 BOTTLE | Historical |