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=ANDA211732"
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
69230-318-05 69230-318 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20201029 N/A ANDA ANDA211732 Camber Consumer Care Inc OMEPRAZOLE 20 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (69230-318-05)
69230-318-10 69230-318 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20201029 N/A ANDA ANDA211732 Camber Consumer Care Inc OMEPRAZOLE 20 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (69230-318-10)
69230-318-32 69230-318 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20200325 N/A ANDA ANDA211732 Camber Consumer Care Inc OMEPRAZOLE 20 mg/1 1 BLISTER PACK in 1 CARTON (69230-318-32) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
69230-318-33 69230-318 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20200325 N/A ANDA ANDA211732 Camber Consumer Care Inc OMEPRAZOLE 20 mg/1 2 BLISTER PACK in 1 CARTON (69230-318-33) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
69230-318-34 69230-318 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20200325 N/A ANDA ANDA211732 Camber Consumer Care Inc OMEPRAZOLE 20 mg/1 3 BLISTER PACK in 1 CARTON (69230-318-34) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
69230-318-35 69230-318 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20200325 N/A ANDA ANDA211732 Camber Consumer Care Inc OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (69230-318-35) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
69230-318-36 69230-318 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20200325 N/A ANDA ANDA211732 Camber Consumer Care Inc OMEPRAZOLE 20 mg/1 2 BOTTLE in 1 CARTON (69230-318-36) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
69230-318-37 69230-318 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20200325 N/A ANDA ANDA211732 Camber Consumer Care Inc OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (69230-318-37) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
50090-6888-0 50090-6888 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20231206 N/A ANDA ANDA211732 A-S Medication Solutions OMEPRAZOLE 20 mg/1 2 BOTTLE in 1 CARTON (50090-6888-0) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
83324-011-14 83324-011 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20240510 N/A ANDA ANDA211732 CHAIN DRUG MARKETING ASSOCIATION, INC. OMEPRAZOLE 20 mg/1 1 CONTAINER in 1 CARTON (83324-011-14) / 14 TABLET, DELAYED RELEASE in 1 CONTAINER
83324-011-42 83324-011 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20240510 N/A ANDA ANDA211732 CHAIN DRUG MARKETING ASSOCIATION, INC. OMEPRAZOLE 20 mg/1 3 CONTAINER in 1 CARTON (83324-011-42) / 14 TABLET, DELAYED RELEASE in 1 CONTAINER
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase