| NDC Code | 50742-657-28 |
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| Package Description | 1 BLISTER PACK in 1 CARTON (50742-657-28) / 28 TABLET in 1 BLISTER PACK (50742-657-01) |
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| Product NDC | 50742-657 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Estradiol And Norethindrone Acetate |
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| Non-Proprietary Name | Estradiol And Norethindrone Acetate |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20190403 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA210612 |
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| Manufacturer | Ingenus Pharmaceuticals, LLC |
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| Substance Name | ESTRADIOL; NORETHINDRONE ACETATE |
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| Strength | 1; .5 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC], Progesterone Congeners [CS], Progestin [EPC] |
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