Finasteride
- Product NDC
- 68788-6976
- 11-digit product format
- 687886976
- Labeler code
- 68788
- Product ID
- 68788-6976_4c078cce-9b63-4f0e-ac7d-182da9a25b8d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmacetucals Inc.
- Application
- ANDA090121
- Marketing category
- ANDA
- Marketing start
- 2017-06-06
- Marketing end
- 0000-00-00
- Substance
- FINASTERIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- 5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68788-6976-1 | 68788697601 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-6976-1) | 2017-06-06 | 0000-00-00 | No | No | Current |
| 68788-6976-3 | 68788697603 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-6976-3) | 2017-06-06 | 0000-00-00 | No | No | Current |
| 68788-6976-6 | 68788697606 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-6976-6) | 2017-06-06 | 0000-00-00 | No | No | Current |
| 68788-6976-9 | 68788697609 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-6976-9) | 2017-06-06 | 0000-00-00 | No | No | Current |