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=ANDA086242"
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
23155-001-01 23155-001 HUMAN PRESCRIPTION DRUG HYDRALAZINE HYDROCHLORIDE hydralazine hydrochloride TABLET, FILM COATED ORAL 20070406 20260831 ANDA ANDA086242 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. HYDRALAZINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (23155-001-01)
55289-133-60 55289-133 HUMAN PRESCRIPTION DRUG HYDRALAZINE HYDROCHLORIDE hydralazine hydrochloride TABLET, FILM COATED ORAL 20220624 N/A ANDA ANDA086242 PD-Rx Pharmaceuticals, Inc. HYDRALAZINE HYDROCHLORIDE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-133-60)
43063-392-90 43063-392 HUMAN PRESCRIPTION DRUG HYDRALAZINE HYDROCHLORIDE hydralazine hydrochloride TABLET, FILM COATED ORAL 20110315 N/A ANDA ANDA086242 PD-Rx Pharmaceuticals, Inc. HYDRALAZINE HYDROCHLORIDE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-392-90)
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