| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 63629-2055-1 | 63629-2055 | HUMAN PRESCRIPTION DRUG | Labetalol Hydrochloride | Labetalol Hydrochloride | TABLET, FILM COATED | ORAL | 20210126 | N/A | ANDA | ANDA207863 | Bryant Ranch Prepack | LABETALOL HYDROCHLORIDE | 300 mg/1 | 500 TABLET, FILM COATED in 1 BOTTLE (63629-2055-1) |
| 63629-2054-1 | 63629-2054 | HUMAN PRESCRIPTION DRUG | Labetalol Hydrochloride | Labetalol Hydrochloride | TABLET, FILM COATED | ORAL | 20210126 | N/A | ANDA | ANDA207863 | Bryant Ranch Prepack | LABETALOL HYDROCHLORIDE | 300 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-2054-1) |
| 63629-2053-1 | 63629-2053 | HUMAN PRESCRIPTION DRUG | Labetalol Hydrochloride | Labetalol Hydrochloride | TABLET, FILM COATED | ORAL | 20210202 | N/A | ANDA | ANDA207863 | Bryant Ranch Prepack | LABETALOL HYDROCHLORIDE | 200 mg/1 | 500 TABLET, FILM COATED in 1 BOTTLE (63629-2053-1) |