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
41520-915-74 41520-915 HUMAN OTC DRUG care one omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20080229 N/A NDA NDA022032 American Sales Company OMEPRAZOLE 20 mg/1 14 BLISTER PACK in 1 CARTON (41520-915-74) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
11822-1190-1 11822-1190 HUMAN OTC DRUG omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20220413 N/A NDA NDA022032 Rite Aid Corporation OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (11822-1190-1) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (11822-1190-0)
55910-215-03 55910-215 HUMAN OTC DRUG dg health omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20210513 N/A NDA NDA022032 Dolgencorp Inc OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (55910-215-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
42507-414-01 42507-414 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20260128 N/A NDA NDA022032 HyVee Inc OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (42507-414-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (42507-414-00)
42507-414-42 42507-414 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20260128 N/A NDA NDA022032 HyVee Inc OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (42507-414-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (42507-414-00)
56062-401-01 56062-401 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20220711 N/A NDA NDA022032 Publix Super Markets Inc OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (56062-401-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
56062-401-03 56062-401 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20220701 N/A NDA NDA022032 Publix Super Markets Inc OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (56062-401-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
37808-915-01 37808-915 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20110204 N/A NDA NDA022032 H E B OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (37808-915-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
37808-915-03 37808-915 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20210427 N/A NDA NDA022032 H E B OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (37808-915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
37808-915-30 37808-915 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20080229 N/A NDA NDA022032 H E B OMEPRAZOLE 20 mg/1 2 CARTON in 1 CARTON (37808-915-30) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
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 (59640-047-01)
0113-0915-01 0113-0915 HUMAN OTC DRUG Good Sense Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20080228 N/A NDA NDA022032 L. Perrigo Company OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (0113-0915-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
0113-0915-03 0113-0915 HUMAN OTC DRUG Good Sense Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20170608 N/A NDA NDA022032 L. Perrigo Company OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (0113-0915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
0113-0915-30 0113-0915 HUMAN OTC DRUG Good Sense Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20080228 N/A NDA NDA022032 L. Perrigo Company OMEPRAZOLE 20 mg/1 2 CARTON in 1 CARTON (0113-0915-30) / 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
41520-802-03 41520-802 HUMAN OTC DRUG careone omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20210311 N/A NDA NDA022032 American Sales Company OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (41520-802-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (41520-802-01)
11673-915-01 11673-915 HUMAN OTC DRUG up and up omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20130813 N/A NDA NDA022032 Target Corporation OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (11673-915-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
11673-915-03 11673-915 HUMAN OTC DRUG up and up omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20130814 N/A NDA NDA022032 Target Corporation OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (11673-915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
11822-0453-1 11822-0453 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20150326 20260801 NDA NDA022032 Rite Aid Corporation OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (11822-0453-1) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
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