| NDC Code | 68462-132-81 |
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| Package Description | 3 POUCH in 1 CARTON (68462-132-81) / 1 BLISTER PACK in 1 POUCH (68462-132-79) / 21 TABLET in 1 BLISTER PACK |
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| Product NDC | 68462-132 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Norethindrone Acetate And Ethinyl Estradiol |
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| Non-Proprietary Name | Norethindrone Acetate And Ethinyl Estradiol |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20160120 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA206969 |
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| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
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| Substance Name | ETHINYL ESTRADIOL; NORETHINDRONE ACETATE |
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| Strength | .02; 1 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Estrogen Receptor Agonists [MoA], Estrogen [EPC], Progesterone Congeners [CS], Progestin [EPC] |
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