| NDC Code | 0555-9009-42 |
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| Package Description | 3 POUCH in 1 CARTON (0555-9009-42) > 1 BLISTER PACK in 1 POUCH (0555-9009-80) > 21 TABLET in 1 BLISTER PACK |
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| Product NDC | 0555-9009 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Nortrel |
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| Proprietary Name Suffix | 21 Day |
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| Non-Proprietary Name | Norethindrone And Ethinyl Estradiol |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20010613 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA072693 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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| Substance Name | ETHINYL ESTRADIOL; NORETHINDRONE |
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| Strength | .035; 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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