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PROPECIA
PROPECIA - 0006-0071-07 - (finasteride)
Drug Information of PROPECIA
| Product NDC: | 0006-0071 |
| Proprietary Name: | PROPECIA |
| 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 PROPECIA
| Product NDC: | 0006-0071 |
| Labeler Name: | Merck Sharp & Dohme Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020788 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19971219 |
Package Information of PROPECIA
| Package NDC: | 0006-0071-07 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (0006-0071-07) > 7 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of PROPECIA
| NDC Code | 0006-0071-07 |
| Proprietary Name | PROPECIA |
| Package Description | 1 BLISTER PACK in 1 CARTON (0006-0071-07) > 7 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 0006-0071 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | finasteride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19971219 |
| Marketing Category Name | NDA |
| Labeler Name | Merck Sharp & Dohme Corp. |
| Substance Name | FINASTERIDE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA] |
