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=ANDA090510"
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
71335-0067-4 71335-0067 HUMAN PRESCRIPTION DRUG hydrochlorothiazide hydrochlorothiazide CAPSULE ORAL 20200812 N/A ANDA ANDA090510 Bryant Ranch Prepack HYDROCHLOROTHIAZIDE 12.5 mg/1 100 CAPSULE in 1 BOTTLE (71335-0067-4)
71335-0067-1 71335-0067 HUMAN PRESCRIPTION DRUG hydrochlorothiazide hydrochlorothiazide CAPSULE ORAL 20180403 N/A ANDA ANDA090510 Bryant Ranch Prepack HYDROCHLOROTHIAZIDE 12.5 mg/1 30 CAPSULE in 1 BOTTLE (71335-0067-1)
71335-0067-2 71335-0067 HUMAN PRESCRIPTION DRUG hydrochlorothiazide hydrochlorothiazide CAPSULE ORAL 20240529 N/A ANDA ANDA090510 Bryant Ranch Prepack HYDROCHLOROTHIAZIDE 12.5 mg/1 10 CAPSULE in 1 BOTTLE (71335-0067-2)
51655-522-26 51655-522 HUMAN PRESCRIPTION DRUG hydrochlorothiazide hydrochlorothiazide CAPSULE ORAL 20230908 N/A ANDA ANDA090510 Northwind Health Company, LLC HYDROCHLOROTHIAZIDE 12.5 mg/1 90 CAPSULE in 1 BOTTLE, PLASTIC (51655-522-26)
51655-522-52 51655-522 HUMAN PRESCRIPTION DRUG hydrochlorothiazide hydrochlorothiazide CAPSULE ORAL 20220629 N/A ANDA ANDA090510 Northwind Health Company, LLC HYDROCHLOROTHIAZIDE 12.5 mg/1 30 CAPSULE in 1 BOTTLE, PLASTIC (51655-522-52)
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