NDC Code | 68462-657-90 |
Package Description | 90 TABLET in 1 BOTTLE (68462-657-90) |
Product NDC | 68462-657 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Norethindrone Acetate And Ethinyl Estradiol |
Non-Proprietary Name | Norethindrone Acetate And Ethinyl Estradiol |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20150402 |
Marketing Category Name | ANDA |
Application Number | ANDA203038 |
Manufacturer | Glenmark Pharmaceuticals Inc., USA |
Substance Name | ETHINYL ESTRADIOL; NORETHINDRONE ACETATE |
Strength | 5; 1 |
Strength Unit | ug/1; mg/1 |
Pharmacy Classes | Estrogen Receptor Agonists [MoA], Estrogen [EPC], Progesterone Congeners [CS], Progestin [EPC] |