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=ANDA078490"
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
55111-645-01 55111-645 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20140301 N/A ANDA ANDA078490 Dr. Reddy's Laboratories Limited OMEPRAZOLE 40 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-645-01)
55111-645-05 55111-645 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20140301 N/A ANDA ANDA078490 Dr. Reddy's Laboratories Limited OMEPRAZOLE 40 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-645-05)
55111-645-30 55111-645 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20140301 N/A ANDA ANDA078490 Dr. Reddy's Laboratories Limited OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-645-30)
55111-645-34 55111-645 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20150514 N/A ANDA ANDA078490 Dr. Reddy's Laboratories Limited OMEPRAZOLE 40 mg/1 12 BOTTLE in 1 CARTON (55111-645-34) / 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE
55111-645-78 55111-645 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20140301 N/A ANDA ANDA078490 Dr. Reddy's Laboratories Limited OMEPRAZOLE 40 mg/1 10 BLISTER PACK in 1 CARTON (55111-645-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (55111-645-79)
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