Finasteride
- Product NDC
- 63739-495
- 11-digit product format
- 637390495
- Labeler code
- 63739
- Product ID
- 63739-495_da78d7ba-d9de-4b04-b088-640547ae1a98
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- McKesson Packaging Services Business Unit of McKesson Corporation
- Application
- ANDA077914
- Marketing category
- ANDA
- Marketing start
- 2010-11-22
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63739-495-40 | 2021-07-16 | C162847 | 48780-1 | 960f7f55-d97c-8e05-e053-dbdaa90a074a | 344a2e9e-24fa-4550-863e-ff56df0bf15c |
| 63739-495-41 | 2021-07-16 | C162847 | 48780-1 | 960f7f55-d97c-8e05-e053-dbdaa90a074a | 344a2e9e-24fa-4550-863e-ff56df0bf15c |
| 63739-495-43 | 2021-07-16 | C162847 | 48780-1 | 960f7f55-d97c-8e05-e053-dbdaa90a074a | 344a2e9e-24fa-4550-863e-ff56df0bf15c |
| 63739-495-40 | 2019-10-29 | C162847 | 48780-1 | 960f7f55-d97c-8e05-e053-dbdaa90a074a | 344a2e9e-24fa-4550-863e-ff56df0bf15c |
| 63739-495-41 | 2019-10-29 | C162847 | 48780-1 | 960f7f55-d97c-8e05-e053-dbdaa90a074a | 344a2e9e-24fa-4550-863e-ff56df0bf15c |
| 63739-495-43 | 2019-10-29 | C162847 | 48780-1 | 960f7f55-d97c-8e05-e053-dbdaa90a074a | 344a2e9e-24fa-4550-863e-ff56df0bf15c |