| NDC Code | 51991-623-28 |
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| Package Description | 1 BLISTER PACK in 1 CARTON (51991-623-28) / 28 TABLET, FILM COATED in 1 BLISTER PACK |
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| Product NDC | 51991-623 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Estradiol / Norethindrone Acetate |
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| Non-Proprietary Name | Estradiol And Norethindrone Acetate |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20110609 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078324 |
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| Manufacturer | Breckenridge Pharmaceutical, Inc. |
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| Substance Name | ESTRADIOL; NORETHINDRONE ACETATE |
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| Strength | .5; .1 |
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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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