| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 70518-3499-2 | 70518-3499 | HUMAN PRESCRIPTION DRUG | LABETALOL HYDROCHLORIDE | Labetalol Hydrochloride | TABLET, FILM COATED | ORAL | 20220920 | N/A | ANDA | ANDA211953 | REMEDYREPACK INC. | LABETALOL HYDROCHLORIDE | 100 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3499-2) |
| 60760-784-90 | 60760-784 | HUMAN PRESCRIPTION DRUG | LABETALOL HYDROCHLORIDE | Labetalol Hydrochloride | TABLET, FILM COATED | ORAL | 20221025 | N/A | ANDA | ANDA211953 | ST. MARY'S MEDICAL PARK PHARMACY | LABETALOL HYDROCHLORIDE | 100 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-784-90) |