| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 62135-952-90 | 62135-952 | HUMAN PRESCRIPTION DRUG | Meclizine Hydrochloride | Meclizine Hydrochloride | TABLET, FILM COATED | ORAL | 20250304 | N/A | ANDA | ANDA203003 | Chartwell RX, LLC | MECLIZINE HYDROCHLORIDE | 12.5 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-952-90) |
| 62135-953-90 | 62135-953 | HUMAN PRESCRIPTION DRUG | Meclizine Hydrochloride | Meclizine Hydrochloride | TABLET, FILM COATED | ORAL | 20250304 | N/A | ANDA | ANDA203003 | Chartwell RX, LLC | MECLIZINE HYDROCHLORIDE | 25 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-953-90) |
| 62135-954-60 | 62135-954 | HUMAN PRESCRIPTION DRUG | Meclizine Hydrochloride | Meclizine Hydrochloride | TABLET, FILM COATED | ORAL | 20250304 | N/A | ANDA | ANDA203003 | Chartwell RX, LLC | MECLIZINE HYDROCHLORIDE | 50 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (62135-954-60) |