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"
符合检索条件的记录共 93 条，共 5 页，当前第 3 页 ，可点击列名称排序
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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
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)
80425-0278-1 80425-0278 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium DR Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20230330 N/A ANDA ANDA202882 Advanced Rx Pharmacy of Tennessee, LLC PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0278-1)
80425-0278-2 80425-0278 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium DR Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20230228 N/A ANDA ANDA202882 Advanced Rx Pharmacy of Tennessee, LLC PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0278-2)
80425-0278-3 80425-0278 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium DR Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20230228 N/A ANDA ANDA202882 Advanced Rx Pharmacy of Tennessee, LLC PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0278-3)
31722-712-31 31722-712 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Camber Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 20 mg/1 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (31722-712-31)
31722-712-32 31722-712 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Camber Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 20 mg/1 10 TABLET, DELAYED RELEASE in 1 CARTON (31722-712-32)
31722-712-90 31722-712 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Camber Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (31722-712-90)
31722-713-10 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 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (31722-713-10)
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)
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)
76420-669-10 76420-669 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 10 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-10)
76420-669-30 76420-669 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-30)
76420-669-60 76420-669 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-60)
76420-669-90 76420-669 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-90)
51655-744-52 51655-744 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20210709 N/A ANDA ANDA202882 Northwind Health Company, LLC PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-744-52)
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)
50090-5793-2 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 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5793-2)
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