| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-1825-7 | 71335-1825 | HUMAN PRESCRIPTION DRUG | Meclizine Hydrochloride | Meclizine Hydrochloride | TABLET | ORAL | 20220224 | N/A | NDA AUTHORIZED GENERIC | NDA010721 | Bryant Ranch Prepack | MECLIZINE HYDROCHLORIDE | 25 mg/1 | 120 TABLET in 1 BOTTLE (71335-1825-7) |
| 71335-1825-8 | 71335-1825 | HUMAN PRESCRIPTION DRUG | Meclizine Hydrochloride | Meclizine Hydrochloride | TABLET | ORAL | 20220224 | N/A | NDA AUTHORIZED GENERIC | NDA010721 | Bryant Ranch Prepack | MECLIZINE HYDROCHLORIDE | 25 mg/1 | 10 TABLET in 1 BOTTLE (71335-1825-8) |
| 71335-1825-9 | 71335-1825 | HUMAN PRESCRIPTION DRUG | Meclizine Hydrochloride | Meclizine Hydrochloride | TABLET | ORAL | 20220224 | N/A | NDA AUTHORIZED GENERIC | NDA010721 | Bryant Ranch Prepack | MECLIZINE HYDROCHLORIDE | 25 mg/1 | 100 TABLET in 1 BOTTLE (71335-1825-9) |
| 16571-662-01 | 16571-662 | HUMAN PRESCRIPTION DRUG | Meclizine Hydrochloride | Meclizine Hydrochloride | TABLET | ORAL | 20200115 | N/A | NDA AUTHORIZED GENERIC | NDA010721 | Rising Pharma Holdings, Inc. | MECLIZINE HYDROCHLORIDE | 50 mg/1 | 100 TABLET in 1 BOTTLE (16571-662-01) |