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
31722-713-31 31722-713 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Camber Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 40 mg/1 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (31722-713-31)
31722-713-32 31722-713 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Camber Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 40 mg/1 10 TABLET, DELAYED RELEASE in 1 CARTON (31722-713-32)
31722-713-90 31722-713 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Camber Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (31722-713-90)
68788-8644-1 68788-8644 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240501 N/A ANDA ANDA202882 Preferred Pharmaceuticals Inc. PANTOPRAZOLE SODIUM 40 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8644-1)
68788-8644-3 68788-8644 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240501 N/A ANDA ANDA202882 Preferred Pharmaceuticals Inc. PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8644-3)
68788-8644-6 68788-8644 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240501 N/A ANDA ANDA202882 Preferred Pharmaceuticals Inc. PANTOPRAZOLE SODIUM 40 mg/1 60 TABLET, DELAYED RELEASE in 1 CARTON (68788-8644-6)
68788-8644-8 68788-8644 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240501 N/A ANDA ANDA202882 Preferred Pharmaceuticals Inc. PANTOPRAZOLE SODIUM 40 mg/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8644-8)
68788-8644-9 68788-8644 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240501 N/A ANDA ANDA202882 Preferred Pharmaceuticals Inc. PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8644-9)
68071-2215-3 68071-2215 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20200708 N/A ANDA ANDA202882 NuCare Pharmaceuticals,Inc. PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2215-3)
68071-2215-4 68071-2215 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20200708 N/A ANDA ANDA202882 NuCare Pharmaceuticals,Inc. PANTOPRAZOLE SODIUM 40 mg/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2215-4)
71610-653-80 71610-653 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220714 N/A ANDA ANDA202882 Aphena Pharma Solutions - Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 180 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-653-80)
71610-653-30 71610-653 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220714 N/A ANDA ANDA202882 Aphena Pharma Solutions - Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-653-30)
71610-653-53 71610-653 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220714 N/A ANDA ANDA202882 Aphena Pharma Solutions - Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-653-53)
71610-653-60 71610-653 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220714 N/A ANDA ANDA202882 Aphena Pharma Solutions - Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-653-60)
71610-659-09 71610-659 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220825 N/A ANDA ANDA202882 Aphena Pharma Solutions - Tennessee, LLC PANTOPRAZOLE SODIUM 20 mg/1 9000 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-659-09)
71610-659-42 71610-659 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20230217 N/A ANDA ANDA202882 Aphena Pharma Solutions - Tennessee, LLC PANTOPRAZOLE SODIUM 20 mg/1 1800 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-659-42)
68071-2285-6 68071-2285 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20201027 N/A ANDA ANDA202882 NuCare Pharmaceuticals,Inc. PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2285-6)
42708-104-30 42708-104 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20191118 N/A ANDA ANDA202882 QPharma Inc PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (42708-104-30)
50090-5793-0 50090-5793 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20211011 N/A ANDA ANDA202882 A-S Medication Solutions PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5793-0)
50090-5793-1 50090-5793 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20211011 N/A ANDA ANDA202882 A-S Medication Solutions PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5793-1)
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