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=NDA022032"
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
55910-215-01 55910-215 HUMAN OTC DRUG dg health omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20200710 N/A NDA NDA022032 Dolgencorp, LLC OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (55910-215-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
55910-215-02 55910-215 HUMAN OTC DRUG dg health omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20210513 N/A NDA NDA022032 Dolgencorp, LLC OMEPRAZOLE 20 mg/1 2 BOTTLE in 1 CARTON (55910-215-02) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
55910-215-03 55910-215 HUMAN OTC DRUG dg health omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20210513 N/A NDA NDA022032 Dolgencorp, LLC OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (55910-215-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
59640-047-03 59640-047 HUMAN OTC DRUG omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20220328 N/A NDA NDA022032 H E B OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (59640-047-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
0363-6101-03 0363-6101 HUMAN OTC DRUG omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20230309 N/A NDA NDA022032 Walgreen Company OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (0363-6101-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (0363-6101-01)
72476-473-01 72476-473 HUMAN OTC DRUG careone omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20220603 N/A NDA NDA022032 Retail Business Services, LLC OMEPRAZOLE 20 mg/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (72476-473-01)
72476-473-03 72476-473 HUMAN OTC DRUG careone omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20220603 N/A NDA NDA022032 Retail Business Services, LLC OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (72476-473-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
41250-401-03 41250-401 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20150325 N/A NDA NDA022032 Meijer Distribution Inc OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (41250-401-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
41250-401-01 41250-401 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20200203 N/A NDA NDA022032 Meijer Distribution Inc OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (41250-401-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
55910-712-01 55910-712 HUMAN OTC DRUG dg health omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20220608 N/A NDA NDA022032 Dolgencorp Inc OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (55910-712-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
55910-712-03 55910-712 HUMAN OTC DRUG dg health omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20220608 N/A NDA NDA022032 Dolgencorp Inc OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (55910-712-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
76162-470-01 76162-470 HUMAN OTC DRUG topcare omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20220922 N/A NDA NDA022032 Topco Associates LLC OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (76162-470-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
76162-470-03 76162-470 HUMAN OTC DRUG topcare omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20220922 N/A NDA NDA022032 Topco Associates LLC OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (76162-470-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
68391-915-55 68391-915 HUMAN OTC DRUG Berkley and Jensen Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20080228 N/A NDA NDA022032 BJWC OMEPRAZOLE 20 mg/1 3 CARTON in 1 CARTON (68391-915-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
30142-557-01 30142-557 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20101008 N/A NDA NDA022032 Kroger Company OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (30142-557-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
30142-557-03 30142-557 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20120103 N/A NDA NDA022032 Kroger Company OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (30142-557-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
30142-557-30 30142-557 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20080225 N/A NDA NDA022032 Kroger Company OMEPRAZOLE 20 mg/1 2 CARTON in 1 CARTON (30142-557-30) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
30142-557-55 30142-557 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20080225 N/A NDA NDA022032 Kroger Company OMEPRAZOLE 20 mg/1 3 CARTON in 1 CARTON (30142-557-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
30142-557-74 30142-557 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20080225 N/A NDA NDA022032 Kroger Company OMEPRAZOLE 20 mg/1 14 BLISTER PACK in 1 CARTON (30142-557-74) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
79903-113-14 79903-113 HUMAN OTC DRUG equate omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20220727 N/A NDA NDA022032 WALMART INC. OMEPRAZOLE 20 mg/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (79903-113-14)
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