Product NDC: | 0009-0064 |
Proprietary Name: | Provera |
Non Proprietary Name: | medroxyprogesterone acetate |
Active Ingredient(s): | 2.5 mg/1 & nbsp; medroxyprogesterone acetate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0009-0064 |
Labeler Name: | Pharmacia and Upjohn Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA011839 |
Marketing Category: | NDA |
Start Marketing Date: | 19590603 |
Package NDC: | 0009-0064-06 |
Package Description: | 30 TABLET in 1 BOTTLE (0009-0064-06) |
NDC Code | 0009-0064-06 |
Proprietary Name | Provera |
Package Description | 30 TABLET in 1 BOTTLE (0009-0064-06) |
Product NDC | 0009-0064 |
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 | 2.5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |