Product NDC: | 54868-5114 |
Proprietary Name: | Avodart |
Non Proprietary Name: | dutasteride |
Active Ingredient(s): | .5 mg/1 & nbsp; dutasteride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-5114 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021319 |
Marketing Category: | NDA |
Start Marketing Date: | 20040716 |
Package NDC: | 54868-5114-0 |
Package Description: | 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (54868-5114-0) |
NDC Code | 54868-5114-0 |
Proprietary Name | Avodart |
Package Description | 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (54868-5114-0) |
Product NDC | 54868-5114 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | dutasteride |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20040716 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | DUTASTERIDE |
Strength Number | .5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA] |