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=ANDA214272"
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
63739-203-18 63739-203 HUMAN PRESCRIPTION DRUG Atovaquone Atovaquone SUSPENSION ORAL 20240419 N/A ANDA ANDA214272 McKesson Corporation dba SKY Packaging ATOVAQUONE 750 mg/5mL 3 TRAY in 1 CASE (63739-203-18) / 6 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (63739-203-05)
63739-203-42 63739-203 HUMAN PRESCRIPTION DRUG Atovaquone Atovaquone SUSPENSION ORAL 20240419 N/A ANDA ANDA214272 McKesson Corporation dba SKY Packaging ATOVAQUONE 750 mg/5mL 7 TRAY in 1 CASE (63739-203-42) / 6 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (63739-203-05)
0121-1016-18 0121-1016 HUMAN PRESCRIPTION DRUG Atovaquone Atovaquone SUSPENSION ORAL 20240110 N/A ANDA ANDA214272 PAI Holdings, LLC ATOVAQUONE 750 mg/5mL 3 TRAY in 1 CASE (0121-1016-18) / 6 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-1016-05)
0121-1016-42 0121-1016 HUMAN PRESCRIPTION DRUG Atovaquone Atovaquone SUSPENSION ORAL 20240110 N/A ANDA ANDA214272 PAI Holdings, LLC ATOVAQUONE 750 mg/5mL 7 TRAY in 1 CASE (0121-1016-42) / 6 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-1016-05)
42239-001-08 42239-001 HUMAN PRESCRIPTION DRUG Atovaquone Atovaquone SUSPENSION ORAL 20231114 N/A ANDA ANDA214272 Abon Pharmaceuticals, LLC ATOVAQUONE 750 mg/5mL 1 BOTTLE in 1 CARTON (42239-001-08) / 210 mL in 1 BOTTLE
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