| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 51285-127-97 | 51285-127 | HUMAN PRESCRIPTION DRUG | Loestrin 21 Day | Norethindrone Acetate and Ethinyl Estradiol | TABLET | ORAL | 20150226 | N/A | ANDA | ANDA076381 | Teva Women's Health LLC | ETHINYL ESTRADIOL; NORETHINDRONE ACETATE | 30 ug/1; 1.5 mg/1 | 5 POUCH in 1 CARTON (51285-127-97) / 1 BLISTER PACK in 1 POUCH / 21 TABLET in 1 BLISTER PACK |
| 0555-9027-42 | 0555-9027 | HUMAN PRESCRIPTION DRUG | Junel 21 Day | Norethindrone Acetate and Ethinyl Estradiol | TABLET | ORAL | 20030918 | N/A | ANDA | ANDA076381 | Teva Pharmaceuticals USA, Inc. | ETHINYL ESTRADIOL; NORETHINDRONE ACETATE | 30 ug/1; 1.5 mg/1 | 3 POUCH in 1 CARTON (0555-9027-42) / 1 BLISTER PACK in 1 POUCH / 21 TABLET in 1 BLISTER PACK |