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=ANDA205868"
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
68071-5119-3 68071-5119 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20191220 N/A ANDA ANDA205868 NuCare Pharmaceuticals,Inc. LANSOPRAZOLE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-5119-3)
68071-5119-4 68071-5119 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20191220 N/A ANDA ANDA205868 NuCare Pharmaceuticals,Inc. LANSOPRAZOLE 30 mg/1 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-5119-4)
50090-6079-0 50090-6079 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20220919 N/A ANDA ANDA205868 A-S Medication Solutions LANSOPRAZOLE 15 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6079-0)
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