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=ANDA219922"
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
13668-735-30 13668-735 HUMAN PRESCRIPTION DRUG pazopanib pazopanib hydrochloride TABLET, FILM COATED ORAL 20250904 N/A ANDA ANDA219922 Torrent Pharmaceuticals Limited PAZOPANIB HYDROCHLORIDE 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (13668-735-30)
13668-735-60 13668-735 HUMAN PRESCRIPTION DRUG pazopanib pazopanib hydrochloride TABLET, FILM COATED ORAL 20250904 N/A ANDA ANDA219922 Torrent Pharmaceuticals Limited PAZOPANIB HYDROCHLORIDE 400 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (13668-735-60)
13668-735-90 13668-735 HUMAN PRESCRIPTION DRUG pazopanib pazopanib hydrochloride TABLET, FILM COATED ORAL 20250904 N/A ANDA ANDA219922 Torrent Pharmaceuticals Limited PAZOPANIB HYDROCHLORIDE 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (13668-735-90)
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