Finasteride
- Product NDC
- 76420-074
- 11-digit product format
- 764200074
- Labeler code
- 76420
- Product ID
- 76420-074_ead2d1fe-f89c-ee3a-e053-2995a90ac920
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA090060
- Marketing category
- ANDA
- Marketing start
- 2013-07-01
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 57GNO57U7G | FINASTERIDE | 98319-26-7 | FINASTERIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 76420-074-30 | 76420007430 | 30 TABLET, FILM COATED in 1 BOTTLE (76420-074-30) | 2020-01-04 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Finasteride | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2022-10-12 | HUMAN PRESCRIPTION DRUG LABEL | 2 |