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=ANDA072096"
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
70677-1132-2 70677-1132 HUMAN OTC DRUG foster and thrive ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20231031 N/A ANDA ANDA072096 Strategic Sourcing Services LLC IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (70677-1132-2) / 50 TABLET, FILM COATED in 1 BOTTLE
70677-1132-3 70677-1132 HUMAN OTC DRUG foster and thrive ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230915 N/A ANDA ANDA072096 Strategic Sourcing Services LLC IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (70677-1132-3) / 100 TABLET, FILM COATED in 1 BOTTLE
70677-1132-4 70677-1132 HUMAN OTC DRUG foster and thrive ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230915 N/A ANDA ANDA072096 Strategic Sourcing Services LLC IBUPROFEN 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (70677-1132-4)
70677-1132-5 70677-1132 HUMAN OTC DRUG foster and thrive ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230915 N/A ANDA ANDA072096 Strategic Sourcing Services LLC IBUPROFEN 200 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70677-1132-5)
50090-7249-3 50090-7249 HUMAN OTC DRUG good sense ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240923 N/A ANDA ANDA072096 A-S Medication Solutions IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (50090-7249-3) / 24 TABLET, FILM COATED in 1 BOTTLE
50090-7249-8 50090-7249 HUMAN OTC DRUG good sense ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241028 N/A ANDA ANDA072096 A-S Medication Solutions IBUPROFEN 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (50090-7249-8)
73598-1104-1 73598-1104 HUMAN OTC DRUG IBUPROFEN 250 IBUPROFEN TABLET, COATED ORAL 20000202 N/A ANDA ANDA072096 JHK Inc dba American Safety & First Aid IBUPROFEN 200 mg/1 125 PACKET in 1 BOX (73598-1104-1) / 2 TABLET, COATED in 1 PACKET
71205-357-06 71205-357 HUMAN OTC DRUG ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20191112 N/A ANDA ANDA072096 Proficient Rx LP IBUPROFEN 200 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (71205-357-06)
71205-357-24 71205-357 HUMAN OTC DRUG ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210826 N/A ANDA ANDA072096 Proficient Rx LP IBUPROFEN 200 mg/1 24 TABLET, FILM COATED in 1 BOTTLE (71205-357-24)
71205-357-30 71205-357 HUMAN OTC DRUG ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20191112 N/A ANDA ANDA072096 Proficient Rx LP IBUPROFEN 200 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-357-30)
71205-357-50 71205-357 HUMAN OTC DRUG ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20191112 N/A ANDA ANDA072096 Proficient Rx LP IBUPROFEN 200 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (71205-357-50)
71205-357-60 71205-357 HUMAN OTC DRUG ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20191112 N/A ANDA ANDA072096 Proficient Rx LP IBUPROFEN 200 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-357-60)
71205-357-90 71205-357 HUMAN OTC DRUG ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20191112 N/A ANDA ANDA072096 Proficient Rx LP IBUPROFEN 200 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-357-90)
56062-604-71 56062-604 HUMAN OTC DRUG ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20021226 N/A ANDA ANDA072096 Publix Super Markets Inc IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (56062-604-71) / 50 TABLET, FILM COATED in 1 BOTTLE
56062-604-78 56062-604 HUMAN OTC DRUG ibuprofen Ibuprofen TABLET, FILM COATED ORAL 19880915 N/A ANDA ANDA072096 Publix Super Markets Inc IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (56062-604-78) / 100 TABLET, FILM COATED in 1 BOTTLE
56062-604-85 56062-604 HUMAN OTC DRUG ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20000320 N/A ANDA ANDA072096 Publix Super Markets Inc IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (56062-604-85) / 250 TABLET, FILM COATED in 1 BOTTLE
56062-604-90 56062-604 HUMAN OTC DRUG ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20041021 N/A ANDA ANDA072096 Publix Super Markets Inc IBUPROFEN 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (56062-604-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase