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Provera
Provera - 0009-0050-11 - (medroxyprogesterone acetate)
Drug Information of Provera
| Product NDC: | 0009-0050 |
| Proprietary Name: | Provera |
| 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 Provera
| Product NDC: | 0009-0050 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011839 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19590603 |
Package Information of Provera
| Package NDC: | 0009-0050-11 |
| Package Description: | 500 TABLET in 1 BOTTLE (0009-0050-11) |
NDC Information of Provera
| NDC Code | 0009-0050-11 |
| Proprietary Name | Provera |
| Package Description | 500 TABLET in 1 BOTTLE (0009-0050-11) |
| Product NDC | 0009-0050 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | medroxyprogesterone acetate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19590603 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | MEDROXYPROGESTERONE ACETATE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
