| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 70771-1104-5 | 70771-1104 | HUMAN PRESCRIPTION DRUG | Doxycycline hyclate | Doxycycline hyclate | TABLET | ORAL | 20180402 | N/A | ANDA | ANDA207773 | Zydus Lifesciences Limited | DOXYCYCLINE HYCLATE | 100 mg/1 | 500 TABLET in 1 BOTTLE (70771-1104-5) |
| 70771-1104-7 | 70771-1104 | HUMAN PRESCRIPTION DRUG | Doxycycline hyclate | Doxycycline hyclate | TABLET | ORAL | 20180402 | N/A | ANDA | ANDA207773 | Zydus Lifesciences Limited | DOXYCYCLINE HYCLATE | 100 mg/1 | 50 TABLET in 1 BOTTLE (70771-1104-7) |
| 67296-1431-1 | 67296-1431 | HUMAN PRESCRIPTION DRUG | Doxycycline Hyclate | Doxycycline Hyclate | TABLET | ORAL | 20210301 | N/A | ANDA | ANDA207773 | RedPharm Drug, Inc. | DOXYCYCLINE HYCLATE | 100 mg/1 | 14 TABLET in 1 BOTTLE (67296-1431-1) |
| 67296-1431-2 | 67296-1431 | HUMAN PRESCRIPTION DRUG | Doxycycline Hyclate | Doxycycline Hyclate | TABLET | ORAL | 20210301 | N/A | ANDA | ANDA207773 | RedPharm Drug, Inc. | DOXYCYCLINE HYCLATE | 100 mg/1 | 20 TABLET in 1 BOTTLE (67296-1431-2) |