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=ANDA076230"
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
70518-3505-1 70518-3505 HUMAN PRESCRIPTION DRUG Lisinopril and Hydrochlorothiazide Lisinopril and Hydrochlorothiazide Tablets TABLET ORAL 20220922 N/A ANDA ANDA076230 REMEDYREPACK INC. HYDROCHLOROTHIAZIDE; LISINOPRIL 12.5 mg/1; 20 mg/1 30 TABLET in 1 BLISTER PACK (70518-3505-1)
70518-3505-4 70518-3505 HUMAN PRESCRIPTION DRUG Lisinopril and Hydrochlorothiazide Lisinopril and Hydrochlorothiazide Tablets TABLET ORAL 20250320 N/A ANDA ANDA076230 REMEDYREPACK INC. HYDROCHLOROTHIAZIDE; LISINOPRIL 12.5 mg/1; 20 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (70518-3505-4)
50090-6752-0 50090-6752 HUMAN PRESCRIPTION DRUG Lisinopril and Hydrochlorothiazide Lisinopril and Hydrochlorothiazide Tablets TABLET ORAL 20231017 N/A ANDA ANDA076230 A-S Medication Solutions HYDROCHLOROTHIAZIDE; LISINOPRIL 12.5 mg/1; 20 mg/1 90 TABLET in 1 BOTTLE (50090-6752-0)
70518-4516-0 70518-4516 HUMAN PRESCRIPTION DRUG Lisinopril and Hydrochlorothiazide Lisinopril and Hydrochlorothiazide Tablets TABLET ORAL 20251106 N/A ANDA ANDA076230 REMEDYREPACK INC. HYDROCHLOROTHIAZIDE; LISINOPRIL 12.5 mg/1; 10 mg/1 30 TABLET in 1 BLISTER PACK (70518-4516-0)
71205-763-60 71205-763 HUMAN PRESCRIPTION DRUG Lisinopril and Hydrochlorothiazide Lisinopril and Hydrochlorothiazide Tablets TABLET ORAL 20230209 N/A ANDA ANDA076230 Proficient Rx LP HYDROCHLOROTHIAZIDE; LISINOPRIL 12.5 mg/1; 20 mg/1 60 TABLET in 1 BOTTLE (71205-763-60)
71205-763-90 71205-763 HUMAN PRESCRIPTION DRUG Lisinopril and Hydrochlorothiazide Lisinopril and Hydrochlorothiazide Tablets TABLET ORAL 20230209 N/A ANDA ANDA076230 Proficient Rx LP HYDROCHLOROTHIAZIDE; LISINOPRIL 12.5 mg/1; 20 mg/1 90 TABLET in 1 BOTTLE (71205-763-90)
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