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
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
51660-029-14 51660-029 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20190601 N/A ANDA ANDA207891 OHM LABORATORIES INC. OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (51660-029-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
21130-991-28 21130-991 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20190601 N/A ANDA ANDA207891 Living Better Brands LLC OMEPRAZOLE 20 mg/1 2 BLISTER PACK in 1 CARTON (21130-991-28) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
21130-991-44 21130-991 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20190601 N/A ANDA ANDA207891 Living Better Brands LLC OMEPRAZOLE 20 mg/1 1 BLISTER PACK in 1 CARTON (21130-991-44) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
51660-029-27 51660-029 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20190601 N/A ANDA ANDA207891 OHM LABORATORIES INC. OMEPRAZOLE 20 mg/1 2 BOTTLE in 1 CARTON (51660-029-27) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
51660-029-44 51660-029 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20190601 N/A ANDA ANDA207891 OHM LABORATORIES INC. OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (51660-029-44) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
67296-2183-8 67296-2183 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20190601 N/A ANDA ANDA207891 Redpharm Drug OMEPRAZOLE 20 mg/1 2 BOTTLE in 1 CARTON (67296-2183-8) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
57896-659-42 57896-659 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20240523 N/A ANDA ANDA207891 GERI-CARE PHARMACEUTICALS, CORP OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (57896-659-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (57896-659-14)
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
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