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=ANDA202882"
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
72189-112-90 72189-112 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM pantoprazole TABLET, DELAYED RELEASE ORAL 20200612 N/A ANDA ANDA202882 DIRECT RX PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-112-90)
71335-0551-1 71335-0551 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20200915 N/A ANDA ANDA202882 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-1)
71335-0551-2 71335-0551 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20200731 N/A ANDA ANDA202882 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-2)
71335-0551-3 71335-0551 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20200617 N/A ANDA ANDA202882 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-3)
71335-0551-4 71335-0551 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240403 N/A ANDA ANDA202882 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 58 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-4)
71335-0551-5 71335-0551 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220310 N/A ANDA ANDA202882 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-5)
71335-0551-6 71335-0551 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240403 N/A ANDA ANDA202882 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-6)
71335-0551-7 71335-0551 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240403 N/A ANDA ANDA202882 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-7)
71335-0551-8 71335-0551 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240403 N/A ANDA ANDA202882 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-8)
71335-0551-9 71335-0551 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240403 N/A ANDA ANDA202882 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-9)
60760-679-30 60760-679 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220301 N/A ANDA ANDA202882 St Mary's Medical Park Pharmacy PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-679-30)
60760-712-60 60760-712 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20200304 N/A ANDA ANDA202882 St. Mary's Medical Park Pharmacy PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-712-60)
68071-4864-9 68071-4864 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20190424 N/A ANDA ANDA202882 NuCare Pharmaceuticals,Inc. PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4864-9)
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