Finasteride
- Product NDC
- 61919-733
- 11-digit product format
- 619190733
- Labeler code
- 61919
- Product ID
- 61919-733_7fbe9f9e-b560-52d9-e053-2a91aa0a4d6f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA090121
- Marketing category
- ANDA
- Marketing start
- 2019-01-18
- 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
- 2020-12-31
- 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 |
|---|
| 61919-733-90 | 61919073390 | 90 TABLET, FILM COATED in 1 BOTTLE (61919-733-90) | 2019-01-18 | 0000-00-00 | No | No | Current |