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Androxy
Androxy - 0832-0086-00 - (fluoxymesterone)
Drug Information of Androxy
| Product NDC: | 0832-0086 |
| Proprietary Name: | Androxy |
| Non Proprietary Name: | fluoxymesterone |
| Active Ingredient(s): | 10 mg/1 & nbsp; fluoxymesterone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Androxy
| Product NDC: | 0832-0086 |
| Labeler Name: | Upsher-Smith Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088342 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19831021 |
Package Information of Androxy
| Package NDC: | 0832-0086-00 |
| Package Description: | 100 TABLET in 1 BOTTLE (0832-0086-00) |
NDC Information of Androxy
| NDC Code | 0832-0086-00 |
| Proprietary Name | Androxy |
| Package Description | 100 TABLET in 1 BOTTLE (0832-0086-00) |
| Product NDC | 0832-0086 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluoxymesterone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19831021 |
| Marketing Category Name | ANDA |
| Labeler Name | Upsher-Smith Laboratories Inc. |
| Substance Name | FLUOXYMESTERONE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient] |
