Finasteride
- Product NDC
- 70518-2363
- 11-digit product format
- 705182363
- Labeler code
- 70518
- Product ID
- 70518-2363_eedbc877-61f5-6bb6-e053-2995a90a20be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090121
- Marketing category
- ANDA
- Marketing start
- 2019-10-16
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2363-0 | 70518236300 | 100 POUCH in 1 BOX, UNIT-DOSE (70518-2363-0) > 1 TABLET, FILM COATED in 1 POUCH (70518-2363-1) | 100 pouch | 2019-10-16 | 0000-00-00 | No | No | Current |
| 70518-2363-2 | 70518236302 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2363-2) | | 2021-02-26 | 0000-00-00 | No | No | Current |
| 70518-2363-3 | 70518236303 | 30 POUCH in 1 BOX (70518-2363-3) > 1 TABLET, FILM COATED in 1 POUCH (70518-2363-4) | 30 pouch | 2021-11-17 | 0000-00-00 | No | No | Current |
| 70518-2363-5 | 70518236305 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2363-5) | | 2022-01-11 | 0000-00-00 | No | No | Current |