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=ANDA201212"
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
68071-3400-7 68071-3400 HUMAN PRESCRIPTION DRUG DIETHYLPROPION HYDROCHLORIDE DIETHYLPROPION HYDROCHLORIDE TABLET ORAL 20230619 N/A ANDA ANDA201212 NuCare Pharmaceuticals,Inc. DIETHYLPROPION HYDROCHLORIDE 25 mg/1 14 TABLET in 1 BOTTLE (68071-3400-7)
68071-3400-1 68071-3400 HUMAN PRESCRIPTION DRUG DIETHYLPROPION HYDROCHLORIDE DIETHYLPROPION HYDROCHLORIDE TABLET ORAL 20230619 N/A ANDA ANDA201212 NuCare Pharmaceuticals,Inc. DIETHYLPROPION HYDROCHLORIDE 25 mg/1 21 TABLET in 1 BOTTLE (68071-3400-1)
68071-3400-2 68071-3400 HUMAN PRESCRIPTION DRUG DIETHYLPROPION HYDROCHLORIDE DIETHYLPROPION HYDROCHLORIDE TABLET ORAL 20230619 N/A ANDA ANDA201212 NuCare Pharmaceuticals,Inc. DIETHYLPROPION HYDROCHLORIDE 25 mg/1 42 TABLET in 1 BOTTLE (68071-3400-2)
68071-3400-3 68071-3400 HUMAN PRESCRIPTION DRUG DIETHYLPROPION HYDROCHLORIDE DIETHYLPROPION HYDROCHLORIDE TABLET ORAL 20230619 N/A ANDA ANDA201212 NuCare Pharmaceuticals,Inc. DIETHYLPROPION HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE (68071-3400-3)
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