Finasteride
- Product NDC
- 50090-1718
- 11-digit product format
- 500901718
- Labeler code
- 50090
- Product ID
- 50090-1718_e20deff0-183a-4afc-afb5-62c8e7fe6738
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090121
- Marketing category
- ANDA
- Marketing start
- 2010-05-28
- 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 |
|---|
| 50090-1718-0 | 50090171800 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-1718-0) | 2015-02-26 | 0000-00-00 | No | No | Current |
| 50090-1718-1 | 50090171801 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-1718-1) | 2015-02-26 | 0000-00-00 | No | No | Current |
| 50090-1718-2 | 50090171802 | 100 TABLET, FILM COATED in 1 BOTTLE (50090-1718-2) | 2015-02-26 | 0000-00-00 | No | No | Current |