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FINASTERIDE
FINASTERIDE - 47335-715-13 - (FINASTERIDE)
Drug Information of FINASTERIDE
| Product NDC: | 47335-715 |
| Proprietary Name: | FINASTERIDE |
| Non Proprietary Name: | FINASTERIDE |
| Active Ingredient(s): | 5 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: | 47335-715 |
| Labeler Name: | Sun Pharma Global FZE |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090507 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110818 |
Package Information of FINASTERIDE
| Package NDC: | 47335-715-13 |
| Package Description: | 500 TABLET, FILM COATED in 1 BOTTLE (47335-715-13) |
NDC Information of FINASTERIDE
| NDC Code | 47335-715-13 |
| Proprietary Name | FINASTERIDE |
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (47335-715-13) |
| Product NDC | 47335-715 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FINASTERIDE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110818 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global FZE |
| Substance Name | FINASTERIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA] |
