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=ANDA078878"
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
49035-397-52 49035-397 HUMAN OTC DRUG Omeprazole Magnesium Omeprazole Magnesium 20.6mg Capsules CAPSULE, DELAYED RELEASE ORAL 20100115 N/A ANDA ANDA078878 Wal-Mart Stores Inc OMEPRAZOLE MAGNESIUM 20 mg/1 1 BOTTLE in 1 CARTON (49035-397-52) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
63868-177-15 63868-177 HUMAN OTC DRUG Omeprazole Magnesium Omeprazole Magnesium CAPSULE, DELAYED RELEASE ORAL 20160101 N/A ANDA ANDA078878 Chain Drug Marketing Association OMEPRAZOLE MAGNESIUM 20 mg/1 1 BOTTLE in 1 CARTON (63868-177-15) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
63868-177-42 63868-177 HUMAN OTC DRUG Omeprazole Magnesium Omeprazole Magnesium CAPSULE, DELAYED RELEASE ORAL 20160101 N/A ANDA ANDA078878 Chain Drug Marketing Association OMEPRAZOLE MAGNESIUM 20 mg/1 3 BOTTLE in 1 CARTON (63868-177-42) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
43598-813-14 43598-813 HUMAN OTC DRUG Omeprazole Magnesium Omeprazole Magnesium CAPSULE, DELAYED RELEASE ORAL 20181226 N/A ANDA ANDA078878 Dr. Reddy's Laboratories Inc. OMEPRAZOLE MAGNESIUM 20 mg/1 1 BOTTLE in 1 CARTON (43598-813-14) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
43598-813-33 43598-813 HUMAN OTC DRUG Omeprazole Magnesium Omeprazole Magnesium CAPSULE, DELAYED RELEASE ORAL 20181226 N/A ANDA ANDA078878 Dr. Reddy's Laboratories Inc. OMEPRAZOLE MAGNESIUM 20 mg/1 3 BOTTLE in 1 CARTON (43598-813-33) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
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