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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
71205-374-30 | 71205-374 | HUMAN PRESCRIPTION DRUG | Meclizine hydrochloride | Meclizine hydrochloride | TABLET | ORAL | 20191217 | N/A | ANDA | ANDA205136 | Proficient Rx LP | MECLIZINE HYDROCHLORIDE | 25 mg/1 | 30 TABLET in 1 BOTTLE (71205-374-30) |
71205-374-60 | 71205-374 | HUMAN PRESCRIPTION DRUG | Meclizine hydrochloride | Meclizine hydrochloride | TABLET | ORAL | 20191217 | N/A | ANDA | ANDA205136 | Proficient Rx LP | MECLIZINE HYDROCHLORIDE | 25 mg/1 | 60 TABLET in 1 BOTTLE (71205-374-60) |
71205-374-90 | 71205-374 | HUMAN PRESCRIPTION DRUG | Meclizine hydrochloride | Meclizine hydrochloride | TABLET | ORAL | 20191217 | N/A | ANDA | ANDA205136 | Proficient Rx LP | MECLIZINE HYDROCHLORIDE | 25 mg/1 | 90 TABLET in 1 BOTTLE (71205-374-90) |