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
76420-671-60 76420-671 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-60)
76420-671-90 76420-671 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-90)
76420-674-01 76420-674 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-674-01)
76420-674-10 76420-674 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 10 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-674-10)
76420-674-30 76420-674 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-674-30)
76420-674-60 76420-674 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-674-60)
76420-674-90 76420-674 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-674-90)
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)
63187-831-30 63187-831 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20170403 N/A ANDA ANDA202882 Proficient Rx LP PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-831-30)
63187-831-60 63187-831 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20170403 N/A ANDA ANDA202882 Proficient Rx LP PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-831-60)
63187-831-90 63187-831 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20170403 N/A ANDA ANDA202882 Proficient Rx LP PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-831-90)
68788-7798-1 68788-7798 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20201013 N/A ANDA ANDA202882 Preferred Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 20 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7798-1)
68788-7798-3 68788-7798 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20201013 N/A ANDA ANDA202882 Preferred Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7798-3)
68788-7798-6 68788-7798 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20201013 N/A ANDA ANDA202882 Preferred Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7798-6)
68788-7798-8 68788-7798 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20201013 N/A ANDA ANDA202882 Preferred Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 20 mg/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7798-8)
68788-7798-9 68788-7798 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20201013 N/A ANDA ANDA202882 Preferred Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7798-9)
72189-112-30 72189-112 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM pantoprazole TABLET, DELAYED RELEASE ORAL 20200612 N/A ANDA ANDA202882 DIRECT RX PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-112-30)
72189-112-60 72189-112 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM pantoprazole TABLET, DELAYED RELEASE ORAL 20200612 N/A ANDA ANDA202882 DIRECT RX PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-112-60)
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)
72865-229-90 72865-229 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220501 N/A ANDA ANDA202882 XLCare Pharmaceuticals Inc. PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-229-90)
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