PROSCAR
- Product NDC
- 0006-0072
- 11-digit product format
- 000060072
- Labeler code
- 0006
- Product ID
- 0006-0072_2745aa4b-c40a-48c3-9d50-85c0876bd478
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FINASTERIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Merck Sharp & Dohme Corp.
- Application
- NDA020180
- Marketing category
- NDA
- Marketing start
- 1992-06-19
- 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
- 2022-12-31
- 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 |
|---|
| 0006-0072-31 | 00006007231 | 30 TABLET, FILM COATED in 1 BOTTLE (0006-0072-31) | 1992-06-19 | 0000-00-00 | No | No | Current |
| 0006-0072-58 | 00006007258 | 100 TABLET, FILM COATED in 1 BOTTLE (0006-0072-58) | 1992-06-19 | 0000-00-00 | No | No | Current |