Finasteride
- Product NDC
- 71335-0281
- 11-digit product format
- 713350281
- Labeler code
- 71335
- Product ID
- 71335-0281_1a867fa6-c569-4b21-8908-249f05f8cc86
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203687
- Marketing category
- ANDA
- Marketing start
- 2014-09-20
- 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
- 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 |
|---|
| 71335-0281-1 | 71335028101 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0281-1) | 2017-07-12 | 0000-00-00 | No | No | Current |
| 71335-0281-2 | 71335028102 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0281-2) | 2017-07-12 | 0000-00-00 | No | No | Current |
| 71335-0281-3 | 71335028103 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0281-3) | 2017-07-12 | 0000-00-00 | No | No | Current |
| 71335-0281-4 | 71335028104 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-0281-4) | 2017-07-12 | 0000-00-00 | No | No | Current |
| 71335-0281-5 | 71335028105 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-0281-5) | 2017-07-12 | 0000-00-00 | No | No | Current |