| NDC Code | 59762-0055-2 |
|---|
| Package Description | 1000 TABLET in 1 BOTTLE (59762-0055-2) |
|---|
| Product NDC | 59762-0055 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Medroxyprogesterone Acetate |
|---|
| Non-Proprietary Name | Medroxyprogesterone Acetate |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20180819 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA011839 |
|---|
| Manufacturer | Mylan Pharmaceuticals Inc. |
|---|
| Substance Name | MEDROXYPROGESTERONE ACETATE |
|---|
| Strength | 2.5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Progesterone Congeners [CS], Progestin [EPC] |
|---|