Finasteride
- Product NDC
- 70518-0397
- 11-digit product format
- 705180397
- Labeler code
- 70518
- Product ID
- 70518-0397_e78ec63d-68fe-5741-e053-2995a90a5042
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090121
- Marketing category
- ANDA
- Marketing start
- 2017-04-04
- 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 |
|---|
| 70518-0397-0 | 70518039700 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0397-0) | 2017-04-04 | 0000-00-00 | No | No | Current |
| 70518-0397-1 | 70518039701 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0397-1) | 2017-04-10 | 0000-00-00 | No | No | Current |
| 70518-0397-2 | 70518039702 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0397-2) | 2018-05-11 | 0000-00-00 | No | No | Current |