FINASTERIDE
- Product NDC
- 76519-1204
- 11-digit product format
- 765191204
- Labeler code
- 76519
- Product ID
- 76519-1204_7432df12-3820-7db6-e053-2991aa0a810a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FINASTERIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- H.J. Harkins Company, Inc.
- Application
- ANDA091643
- Marketing category
- ANDA
- Marketing start
- 2018-04-26
- 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
- 2019-12-31
- 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 |
|---|
| 76519-1204-3 | FINASTERIDE | 30 in 1 VIAL, PLASTIC | TABLET, FILM COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76519-1204 | FINASTERIDE TABLET, FILM COATED [H.J. HARKINS COMPANY, INC.] | 1 | Legacy NDC, 1 package rows | 20180825_7432df12-381f-7db6-e053-2991aa0a810a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 76519-1204-3 | 76519120403 | 30 in 1 VIAL, PLASTIC | Historical |