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Finasteride
Finasteride - 55111-172-90 - (Finasteride)
Drug Information of Finasteride
| Product NDC: | 55111-172 |
| Proprietary Name: | Finasteride |
| Non Proprietary Name: | Finasteride |
| Active Ingredient(s): | 5 mg/1 & nbsp; Finasteride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Finasteride
| Product NDC: | 55111-172 |
| Labeler Name: | Dr. Reddy's Laboratories Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076437 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070228 |
Package Information of Finasteride
| Package NDC: | 55111-172-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (55111-172-90) |
NDC Information of Finasteride
| NDC Code | 55111-172-90 |
| Proprietary Name | Finasteride |
| Package Description | 90 TABLET in 1 BOTTLE (55111-172-90) |
| Product NDC | 55111-172 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Finasteride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070228 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr. Reddy's Laboratories Limited |
| Substance Name | FINASTERIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA] |
