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Flutamide
Flutamide - 49884-753-13 - (Flutamide)
Drug Information of Flutamide
| Product NDC: | 49884-753 |
| Proprietary Name: | Flutamide |
| Non Proprietary Name: | Flutamide |
| Active Ingredient(s): | 125 mg/1 & nbsp; Flutamide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Flutamide
| Product NDC: | 49884-753 |
| Labeler Name: | Par Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075298 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010918 |
Package Information of Flutamide
| Package NDC: | 49884-753-13 |
| Package Description: | 180 CAPSULE in 1 BOTTLE (49884-753-13) |
NDC Information of Flutamide
| NDC Code | 49884-753-13 |
| Proprietary Name | Flutamide |
| Package Description | 180 CAPSULE in 1 BOTTLE (49884-753-13) |
| Product NDC | 49884-753 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Flutamide |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20010918 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Inc. |
| Substance Name | FLUTAMIDE |
| Strength Number | 125 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Androgen Receptor Antagonists [MoA],Androgen Receptor Inhibitor [EPC] |
