| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 67296-1432-3 | 67296-1432 | HUMAN PRESCRIPTION DRUG | Meclizine Hydrochloride | Meclizine Hydrochloride | TABLET | ORAL | 20210301 | N/A | NDA AUTHORIZED GENERIC | NDA010721 | RedPharm Drug, Inc. | MECLIZINE HYDROCHLORIDE | 25 mg/1 | 30 TABLET in 1 BOTTLE (67296-1432-3) |
| 67296-1432-7 | 67296-1432 | HUMAN PRESCRIPTION DRUG | Meclizine Hydrochloride | Meclizine Hydrochloride | TABLET | ORAL | 20200115 | N/A | NDA AUTHORIZED GENERIC | NDA010721 | RedPharm Drug, Inc. | MECLIZINE HYDROCHLORIDE | 25 mg/1 | 21 TABLET in 1 BOTTLE (67296-1432-7) |