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=ANDA211852"
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
69097-391-02 69097-391 HUMAN PRESCRIPTION DRUG deferasirox deferasirox TABLET, COATED ORAL 20200213 N/A ANDA ANDA211852 Cipla USA Inc. DEFERASIROX 90 mg/1 30 TABLET, COATED in 1 BOTTLE (69097-391-02)
69097-391-20 69097-391 HUMAN PRESCRIPTION DRUG deferasirox deferasirox TABLET, COATED ORAL 20200213 N/A ANDA ANDA211852 Cipla USA Inc. DEFERASIROX 90 mg/1 5 BLISTER PACK in 1 CARTON (69097-391-20) / 10 TABLET, COATED in 1 BLISTER PACK (69097-391-19)
69097-392-02 69097-392 HUMAN PRESCRIPTION DRUG deferasirox deferasirox TABLET, COATED ORAL 20200614 N/A ANDA ANDA211852 Cipla USA Inc. DEFERASIROX 180 mg/1 30 TABLET, COATED in 1 BOTTLE (69097-392-02)
69097-392-20 69097-392 HUMAN PRESCRIPTION DRUG deferasirox deferasirox TABLET, COATED ORAL 20200614 N/A ANDA ANDA211852 Cipla USA Inc. DEFERASIROX 180 mg/1 5 BLISTER PACK in 1 CARTON (69097-392-20) / 10 TABLET, COATED in 1 BLISTER PACK (69097-392-19)
69097-393-02 69097-393 HUMAN PRESCRIPTION DRUG deferasirox deferasirox TABLET, COATED ORAL 20200213 N/A ANDA ANDA211852 Cipla USA Inc. DEFERASIROX 360 mg/1 30 TABLET, COATED in 1 BOTTLE (69097-393-02)
69097-393-20 69097-393 HUMAN PRESCRIPTION DRUG deferasirox deferasirox TABLET, COATED ORAL 20200213 N/A ANDA ANDA211852 Cipla USA Inc. DEFERASIROX 360 mg/1 5 BLISTER PACK in 1 CARTON (69097-393-20) / 10 TABLET, COATED in 1 BLISTER PACK (69097-393-19)
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