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=ANDA078391"
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
71610-139-60 71610-139 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide CAPSULE, GELATIN COATED ORAL 20180830 N/A ANDA ANDA078391 Aphena Pharma Solutions - Tennessee, LLC HYDROCHLOROTHIAZIDE 12.5 mg/1 90 CAPSULE, GELATIN COATED in 1 BOTTLE (71610-139-60)
59746-382-06 59746-382 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide CAPSULE, GELATIN COATED ORAL 20080211 N/A ANDA ANDA078391 JUBILANT CADISTA PHARMACEUTICALS INC. HYDROCHLOROTHIAZIDE 12.5 mg/1 100 CAPSULE, GELATIN COATED in 1 BOTTLE (59746-382-06)
59746-382-10 59746-382 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide CAPSULE, GELATIN COATED ORAL 20080211 N/A ANDA ANDA078391 JUBILANT CADISTA PHARMACEUTICALS INC. HYDROCHLOROTHIAZIDE 12.5 mg/1 1000 CAPSULE, GELATIN COATED in 1 BOTTLE (59746-382-10)
59746-382-05 59746-382 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide CAPSULE, GELATIN COATED ORAL 20080211 N/A ANDA ANDA078391 JUBILANT CADISTA PHARMACEUTICALS INC. HYDROCHLOROTHIAZIDE 12.5 mg/1 30 CAPSULE, GELATIN COATED in 1 BOTTLE (59746-382-05)
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