Home
>
National Drug Code (NDC)
>
Finasteride
Finasteride - 47335-714-88 - (Finasteride)
Drug Information of Finasteride
| Product NDC: | 47335-714 |
| Proprietary Name: | Finasteride |
| Non Proprietary Name: | Finasteride |
| Active Ingredient(s): | 1 mg/1 & nbsp; Finasteride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Finasteride
| Product NDC: | 47335-714 |
| Labeler Name: | Sun Pharma Global FZE |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090508 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130701 |
Package Information of Finasteride
| Package NDC: | 47335-714-88 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (47335-714-88) |
NDC Information of Finasteride
| NDC Code | 47335-714-88 |
| Proprietary Name | Finasteride |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (47335-714-88) |
| Product NDC | 47335-714 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Finasteride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130701 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global FZE |
| Substance Name | FINASTERIDE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA] |
