| Product NDC: | 54868-2985 |
| Proprietary Name: | MEDROXYPROGESTERONE ACETATE |
| Non Proprietary Name: | medroxyprogesterone acetate |
| Active Ingredient(s): | 5 mg/1 & nbsp; medroxyprogesterone acetate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54868-2985 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011839 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19950919 |
| Package NDC: | 54868-2985-3 |
| Package Description: | 90 TABLET in 1 BOTTLE, PLASTIC (54868-2985-3) |
| NDC Code | 54868-2985-3 |
| Proprietary Name | MEDROXYPROGESTERONE ACETATE |
| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (54868-2985-3) |
| Product NDC | 54868-2985 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | medroxyprogesterone acetate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19950919 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | MEDROXYPROGESTERONE ACETATE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |