| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 63629-1164-1 | 63629-1164 | HUMAN PRESCRIPTION DRUG | Labetalol Hydrochloride | Labetalol Hydrochloride | TABLET, FILM COATED | ORAL | 20201002 | N/A | ANDA | ANDA075215 | Bryant Ranch Prepack | LABETALOL | 200 mg/1 | 500 TABLET, FILM COATED in 1 BOTTLE (63629-1164-1) |
| 63629-1165-1 | 63629-1165 | HUMAN PRESCRIPTION DRUG | Labetalol Hydrochloride | Labetalol Hydrochloride | TABLET, FILM COATED | ORAL | 20191122 | N/A | ANDA | ANDA075215 | Bryant Ranch Prepack | LABETALOL | 300 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-1165-1) |
| 63629-1166-1 | 63629-1166 | HUMAN PRESCRIPTION DRUG | Labetalol Hydrochloride | Labetalol Hydrochloride | TABLET, FILM COATED | ORAL | 20191122 | N/A | ANDA | ANDA075215 | Bryant Ranch Prepack | LABETALOL | 300 mg/1 | 500 TABLET, FILM COATED in 1 BOTTLE (63629-1166-1) |