| NDC Code | 0603-7607-48 |
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| Package Description | 3 BLISTER PACK in 1 CARTON (0603-7607-48) > 21 TABLET, FILM COATED in 1 BLISTER PACK (0603-7607-02) |
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| Product NDC | 0603-7607 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Gildess 1/20 |
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| Non-Proprietary Name | Norethindrone Acetate And Ethinyl Estradiol |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20120724 |
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| End Marketing Date | 20180331 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077077 |
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| Manufacturer | Par Pharmaceutical |
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| Substance Name | NORETHINDRONE ACETATE; ETHINYL ESTRADIOL |
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| Strength | 1; .02 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
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