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MEDROXYPROGESTERONE ACETATE
MEDROXYPROGESTERONE ACETATE - 54868-0109-0 - (medroxyprogesterone acetate)
Drug Information of MEDROXYPROGESTERONE ACETATE
| Product NDC: | 54868-0109 |
| Proprietary Name: | MEDROXYPROGESTERONE ACETATE |
| Non Proprietary Name: | medroxyprogesterone acetate |
| Active Ingredient(s): | 10 mg/1 & nbsp; medroxyprogesterone acetate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MEDROXYPROGESTERONE ACETATE
| Product NDC: | 54868-0109 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011839 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19940706 |
Package Information of MEDROXYPROGESTERONE ACETATE
| Package NDC: | 54868-0109-0 |
| Package Description: | 25 TABLET in 1 BOTTLE, PLASTIC (54868-0109-0) |
NDC Information of MEDROXYPROGESTERONE ACETATE
| NDC Code | 54868-0109-0 |
| Proprietary Name | MEDROXYPROGESTERONE ACETATE |
| Package Description | 25 TABLET in 1 BOTTLE, PLASTIC (54868-0109-0) |
| Product NDC | 54868-0109 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | medroxyprogesterone acetate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19940706 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | MEDROXYPROGESTERONE ACETATE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
