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=ANDA040702"
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
63187-441-90 63187-441 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20140501 N/A ANDA ANDA040702 Proficient Rx LP HYDROCHLOROTHIAZIDE 50 mg/1 90 TABLET in 1 BOTTLE (63187-441-90)
68071-3608-3 68071-3608 HUMAN PRESCRIPTION DRUG HYDROCHLOROTHIAZIDE HYDROCHLOROTHIAZIDE TABLET ORAL 20240515 N/A ANDA ANDA040702 NuCare Pharmaceuticals,Inc. HYDROCHLOROTHIAZIDE 12.5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (68071-3608-3)
50090-6372-0 50090-6372 HUMAN PRESCRIPTION DRUG HYDROCHLOROTHIAZIDE HYDROCHLOROTHIAZIDE TABLET ORAL 20230213 N/A ANDA ANDA040702 A-S Medication Solutions HYDROCHLOROTHIAZIDE 12.5 mg/1 30 TABLET in 1 BOTTLE (50090-6372-0)
50090-6372-2 50090-6372 HUMAN PRESCRIPTION DRUG HYDROCHLOROTHIAZIDE HYDROCHLOROTHIAZIDE TABLET ORAL 20230213 N/A ANDA ANDA040702 A-S Medication Solutions HYDROCHLOROTHIAZIDE 12.5 mg/1 100 TABLET in 1 BOTTLE (50090-6372-2)
50090-6372-3 50090-6372 HUMAN PRESCRIPTION DRUG HYDROCHLOROTHIAZIDE HYDROCHLOROTHIAZIDE TABLET ORAL 20230213 N/A ANDA ANDA040702 A-S Medication Solutions HYDROCHLOROTHIAZIDE 12.5 mg/1 90 TABLET in 1 BOTTLE (50090-6372-3)
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