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=ANDA078281"
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
72162-1746-9 72162-1746 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20240404 N/A ANDA ANDA078281 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-9)
72162-1746-3 72162-1746 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20240404 N/A ANDA ANDA078281 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-3)
43353-027-53 43353-027 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20150429 N/A ANDA ANDA078281 Aphena Pharma Solutions - Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (43353-027-53)
43353-027-60 43353-027 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20160419 N/A ANDA ANDA078281 Aphena Pharma Solutions - Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (43353-027-60)
43353-027-30 43353-027 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20150429 N/A ANDA ANDA078281 Aphena Pharma Solutions - Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (43353-027-30)
55154-4346-0 55154-4346 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20210128 N/A ANDA ANDA078281 Cardinal Health 107, LLC PANTOPRAZOLE SODIUM 20 mg/1 10 BLISTER PACK in 1 BAG (55154-4346-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
43353-027-80 43353-027 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20160419 N/A ANDA ANDA078281 Aphena Pharma Solutions - Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 180 TABLET, DELAYED RELEASE in 1 BOTTLE (43353-027-80)
50268-585-15 50268-585 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20210128 N/A ANDA ANDA078281 AvPAK PANTOPRAZOLE SODIUM 20 mg/1 50 BLISTER PACK in 1 BOX (50268-585-15) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (50268-585-11)
50268-639-15 50268-639 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20150219 N/A ANDA ANDA078281 AvPAK PANTOPRAZOLE SODIUM 40 mg/1 50 BLISTER PACK in 1 BOX (50268-639-15) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (50268-639-11)
63739-564-10 63739-564 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20110120 20260430 ANDA ANDA078281 McKesson Corporation dba SKY Packaging PANTOPRAZOLE SODIUM 40 mg/1 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-564-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
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