美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA216171"
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
71839-122-01 71839-122 HUMAN PRESCRIPTION DRUG Pantoprazole sodium Pantoprazole sodium INJECTION, POWDER, FOR SOLUTION INTRAVENOUS 20220525 N/A ANDA ANDA216171 BE Pharmaceuticals Inc. PANTOPRAZOLE SODIUM 40 mg/10mL 1 VIAL in 1 CARTON (71839-122-01) / 10 mL in 1 VIAL
71839-122-10 71839-122 HUMAN PRESCRIPTION DRUG Pantoprazole sodium Pantoprazole sodium INJECTION, POWDER, FOR SOLUTION INTRAVENOUS 20220525 N/A ANDA ANDA216171 BE Pharmaceuticals Inc. PANTOPRAZOLE SODIUM 40 mg/10mL 10 CARTON in 1 PACKAGE (71839-122-10) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL
71839-122-25 71839-122 HUMAN PRESCRIPTION DRUG Pantoprazole sodium Pantoprazole sodium INJECTION, POWDER, FOR SOLUTION INTRAVENOUS 20220525 N/A ANDA ANDA216171 BE Pharmaceuticals Inc. PANTOPRAZOLE SODIUM 40 mg/10mL 25 CARTON in 1 PACKAGE (71839-122-25) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL
72205-180-07 72205-180 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium INJECTION, POWDER, FOR SOLUTION INTRAVENOUS 20220519 N/A ANDA ANDA216171 Novadoz Pharmaceuticals LLC PANTOPRAZOLE SODIUM 40 mg/10mL 10 VIAL in 1 CARTON (72205-180-07) / 10 mL in 1 VIAL (72205-180-01)
72205-180-09 72205-180 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium INJECTION, POWDER, FOR SOLUTION INTRAVENOUS 20220519 N/A ANDA ANDA216171 Novadoz Pharmaceuticals LLC PANTOPRAZOLE SODIUM 40 mg/10mL 25 VIAL in 1 CARTON (72205-180-09) / 10 mL in 1 VIAL (72205-180-01)
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