| NDC Code | 51285-079-97 |
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| Package Description | 5 BLISTER PACK in 1 CARTON (51285-079-97) > 21 TABLET in 1 BLISTER PACK |
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| Product NDC | 51285-079 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Loestrin 1/20 |
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| Proprietary Name Suffix | 21 Day |
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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 | 20081001 |
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| End Marketing Date | 20151130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076380 |
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| Manufacturer | Teva Women's Health, Inc. |
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| Substance Name | NORETHINDRONE ACETATE; ETHINYL ESTRADIOL |
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| Strength | 1; 20 |
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| Strength Unit | mg/1; ug/1 |
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| Pharmacy Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
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