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=ANDA207891"
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
30142-992-14 30142-992 HUMAN OTC DRUG omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20200715 N/A ANDA ANDA207891 THE KROGER COMPANY OMEPRAZOLE 20 mg/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (30142-992-14)
30142-992-28 30142-992 HUMAN OTC DRUG omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20200715 N/A ANDA ANDA207891 THE KROGER COMPANY OMEPRAZOLE 20 mg/1 2 TABLET, DELAYED RELEASE in 1 CARTON (30142-992-28)
72559-014-06 72559-014 HUMAN OTC DRUG omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20200715 N/A ANDA ANDA207891 Little Pharma, Inc. OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (72559-014-06) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
72559-014-07 72559-014 HUMAN OTC DRUG omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20200715 N/A ANDA ANDA207891 Little Pharma, Inc. OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (72559-014-07) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
72559-014-36 72559-014 HUMAN OTC DRUG omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20240618 N/A ANDA ANDA207891 Little Pharma, Inc. OMEPRAZOLE 20 mg/1 4 CARTON in 1 PACKAGE, COMBINATION (72559-014-36) / 3 BOTTLE in 1 CARTON / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
72036-981-14 72036-981 HUMAN OTC DRUG Omeprazole OMEPRAZOLE TABLET, DELAYED RELEASE ORAL 20200916 N/A ANDA ANDA207891 HARRIS TEETER OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (72036-981-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
72036-981-42 72036-981 HUMAN OTC DRUG Omeprazole OMEPRAZOLE TABLET, DELAYED RELEASE ORAL 20200916 N/A ANDA ANDA207891 HARRIS TEETER OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (72036-981-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
70677-0148-1 70677-0148 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20190101 N/A ANDA ANDA207891 Strategic Sourcing Services OMEPRAZOLE 20 mg/1 1 BLISTER PACK in 1 CARTON (70677-0148-1) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
62756-377-11 62756-377 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20190101 N/A ANDA ANDA207891 Sun Pharmaceutical Industries, Inc. OMEPRAZOLE 20 mg/1 2 BOTTLE in 1 CARTON (62756-377-11) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
62756-377-12 62756-377 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20190101 N/A ANDA ANDA207891 Sun Pharmaceutical Industries, Inc. OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (62756-377-12) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
62756-377-21 62756-377 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20190101 N/A ANDA ANDA207891 Sun Pharmaceutical Industries, Inc. OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (62756-377-21) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
62756-377-70 62756-377 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20190101 N/A ANDA ANDA207891 Sun Pharmaceutical Industries, Inc. OMEPRAZOLE 20 mg/1 1 BLISTER PACK in 1 CARTON (62756-377-70) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
62756-377-79 62756-377 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20190101 N/A ANDA ANDA207891 Sun Pharmaceutical Industries, Inc. OMEPRAZOLE 20 mg/1 3 BLISTER PACK in 1 CARTON (62756-377-79) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
62756-377-96 62756-377 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20190101 N/A ANDA ANDA207891 Sun Pharmaceutical Industries, Inc. OMEPRAZOLE 20 mg/1 2 BLISTER PACK in 1 CARTON (62756-377-96) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
70677-1098-1 70677-1098 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20230811 N/A ANDA ANDA207891 STRATEGIC SOURCING SERVICES LLC OMEPRAZOLE 20 mg/1 1 BLISTER PACK in 1 CARTON (70677-1098-1) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
63941-997-14 63941-997 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20180721 N/A ANDA ANDA207891 VALU MERCHANDISERS COMPANY OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (63941-997-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
63941-997-42 63941-997 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20180721 N/A ANDA ANDA207891 VALU MERCHANDISERS COMPANY OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (63941-997-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
57483-840-42 57483-840 HUMAN OTC DRUG omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20200810 N/A ANDA ANDA207891 INNOVUS PHARMACEUTICALS, INC. OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (57483-840-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (57483-840-01)
55681-306-14 55681-306 HUMAN OTC DRUG Omeprazole OMEPRAZOLE TABLET, DELAYED RELEASE ORAL 20220414 N/A ANDA ANDA207891 Twin Med LLC OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (55681-306-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
55681-306-42 55681-306 HUMAN OTC DRUG Omeprazole OMEPRAZOLE TABLET, DELAYED RELEASE ORAL 20220414 N/A ANDA ANDA207891 Twin Med LLC OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (55681-306-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
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