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
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)
0363-0915-01 0363-0915 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20101006 N/A NDA NDA022032 Walgreen Company OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (0363-0915-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
0363-0915-03 0363-0915 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20110325 N/A NDA NDA022032 Walgreen Company OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (0363-0915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
0363-0915-30 0363-0915 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20080227 N/A NDA NDA022032 Walgreen Company OMEPRAZOLE 20 mg/1 2 CARTON in 1 CARTON (0363-0915-30) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
0363-0915-55 0363-0915 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20080227 N/A NDA NDA022032 Walgreen Company OMEPRAZOLE 20 mg/1 3 CARTON in 1 CARTON (0363-0915-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
70000-0723-1 70000-0723 HUMAN OTC DRUG leader omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20250416 N/A NDA NDA022032 Cardinal Health 110, LLC. dba Leader OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (70000-0723-1) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
70000-0723-2 70000-0723 HUMAN OTC DRUG leader omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20250416 N/A NDA NDA022032 Cardinal Health 110, LLC. dba Leader OMEPRAZOLE 20 mg/1 14 BLISTER PACK in 1 CARTON (70000-0723-2) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
70000-0723-3 70000-0723 HUMAN OTC DRUG leader omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20250416 N/A NDA NDA022032 Cardinal Health 110, LLC. dba Leader OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (70000-0723-3) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
68196-700-01 68196-700 HUMAN OTC DRUG members mark omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20240207 N/A NDA NDA022032 Sam's West Inc OMEPRAZOLE 20 mg/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68196-700-01)
68196-700-03 68196-700 HUMAN OTC DRUG members mark omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20240207 N/A NDA NDA022032 Sam's West Inc OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (68196-700-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
68196-915-55 68196-915 HUMAN OTC DRUG members mark omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20080225 N/A NDA NDA022032 Sam's West Inc OMEPRAZOLE 20 mg/1 3 CARTON in 1 CARTON (68196-915-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
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)
11673-018-01 11673-018 HUMAN OTC DRUG up and up omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20170302 N/A NDA NDA022032 Target Corporation OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (11673-018-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
11673-018-03 11673-018 HUMAN OTC DRUG up and up omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20150417 N/A NDA NDA022032 Target Corporation OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (11673-018-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
37808-401-01 37808-401 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20150403 N/A NDA NDA022032 H E B OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (37808-401-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
37808-401-03 37808-401 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20150403 N/A NDA NDA022032 H E B OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (37808-401-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
11673-346-03 11673-346 HUMAN OTC DRUG up and up omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20220203 N/A NDA NDA022032 Target Corporation OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (11673-346-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
79481-0075-1 79481-0075 HUMAN OTC DRUG 24 hr omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20220525 N/A NDA NDA022032 Meijer, Inc. OMEPRAZOLE 20 mg/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (79481-0075-1)
79481-0075-3 79481-0075 HUMAN OTC DRUG 24 hr omeprazole omeprazole TABLET, DELAYED RELEASE ORAL 20220525 N/A NDA NDA022032 Meijer, Inc. OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (79481-0075-3) / 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
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