Finasteride
- Product NDC
- 76420-153
- 11-digit product format
- 764200153
- Labeler code
- 76420
- Product ID
- 76420-153_c8288b30-929b-1ff7-e053-2995a90ae333
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA203687
- Marketing category
- ANDA
- Marketing start
- 2013-11-05
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76420-153-30 | 76420015330 | 30 TABLET, FILM COATED in 1 BOTTLE (76420-153-30) | 2021-07-28 | 0000-00-00 | No | No | Current |
| 76420-153-90 | 76420015390 | 90 TABLET, FILM COATED in 1 BOTTLE (76420-153-90) | 2021-07-28 | 0000-00-00 | No | No | Current |