| NDC包装代码 | 产品NDC | 产品类型 | 商品名 | 通用名 | 剂型 | 给药途径 | 上市日期 | 结束日期 | 市场类别 | 申请号 | 标签持有者 | 活性成分 | 规格 | 包装描述 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 68462-132-81 | 68462-132 | HUMAN PRESCRIPTION DRUG | Norethindrone Acetate and Ethinyl Estradiol | Norethindrone Acetate and Ethinyl Estradiol | TABLET | ORAL | 20160120 | N/A | ANDA | ANDA206969 | Glenmark Pharmaceuticals Inc., USA | ETHINYL ESTRADIOL; NORETHINDRONE ACETATE | .02 mg/1; 1 mg/1 | 3 POUCH in 1 CARTON (68462-132-81) / 1 BLISTER PACK in 1 POUCH (68462-132-79) / 21 TABLET in 1 BLISTER PACK |
| 50090-6782-0 | 50090-6782 | HUMAN PRESCRIPTION DRUG | Norethindrone Acetate and Ethinyl Estradiol | Norethindrone Acetate and Ethinyl Estradiol | TABLET | ORAL | 20231030 | N/A | ANDA | ANDA206969 | A-S Medication Solutions | ETHINYL ESTRADIOL; NORETHINDRONE ACETATE | .02 mg/1; 1 mg/1 | 1 BLISTER PACK in 1 CARTON (50090-6782-0) / 21 TABLET in 1 BLISTER PACK |