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"
符合检索条件的记录共 131 条，共 7 页，当前第 4 页 ，可点击列名称排序
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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
0113-0915-74 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 14 BLISTER PACK in 1 CARTON (0113-0915-74) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
0113-1723-01 0113-1723 HUMAN OTC DRUG Good Sense Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20190522 N/A NDA NDA022032 L. Perrigo Company OMEPRAZOLE 20 mg/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (0113-1723-01)
0113-1723-03 0113-1723 HUMAN OTC DRUG Good Sense Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20190522 N/A NDA NDA022032 L. Perrigo Company OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (0113-1723-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
0113-1803-03 0113-1803 HUMAN OTC DRUG good sense omeprazole delayed release omeprazole TABLET, DELAYED RELEASE ORAL 20211221 N/A NDA NDA022032 L. Perrigo Company OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (0113-1803-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (0113-1803-01)
0363-0007-01 0363-0007 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20150325 N/A NDA NDA022032 Walgreen Company OMEPRAZOLE 20 mg/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (0363-0007-01)
0363-0007-03 0363-0007 HUMAN OTC DRUG omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20150325 N/A NDA NDA022032 Walgreen Company OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (0363-0007-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
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
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)
0536-1448-13 0536-1448 HUMAN OTC DRUG rugby omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20250415 N/A NDA NDA022032 Rugby Laboratories OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (0536-1448-13) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
0536-1448-88 0536-1448 HUMAN OTC DRUG rugby omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20250415 N/A NDA NDA022032 Rugby Laboratories OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (0536-1448-88) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
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
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
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
30142-593-01 30142-593 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20170209 N/A NDA NDA022032 Kroger Company OMEPRAZOLE 20 mg/1 1 BOTTLE in 1 CARTON (30142-593-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
30142-593-03 30142-593 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20170209 N/A NDA NDA022032 Kroger Company OMEPRAZOLE 20 mg/1 3 BOTTLE in 1 CARTON (30142-593-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
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