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=ANDA090796"
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
51655-275-26 51655-275 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20200616 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-26)
51655-275-54 51655-275 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20200921 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 800 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-54)
73086-211-01 73086-211 HUMAN PRESCRIPTION DRUG ibuprofen ibuprofen TABLET ORAL 20240320 N/A ANDA ANDA090796 SKYA HEALTH, LLC IBUPROFEN 600 mg/1 100 TABLET in 1 BOTTLE (73086-211-01)
49483-602-50 49483-602 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 TIME CAP LABORATORIES, INC IBUPROFEN 400 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (49483-602-50)
60760-603-30 60760-603 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20211020 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-30)
60760-603-40 60760-603 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191226 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 600 mg/1 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-40)
60760-603-60 60760-603 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191021 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-60)
60760-603-90 60760-603 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20230206 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-90)
60760-604-09 60760-604 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200610 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 800 mg/1 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-09)
60760-604-20 60760-604 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191016 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 800 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-20)
43063-867-01 43063-867 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20180711 N/A ANDA ANDA090796 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-01)
43063-867-10 43063-867 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20180905 N/A ANDA ANDA090796 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 600 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-10)
43063-867-30 43063-867 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20231030 N/A ANDA ANDA090796 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-30)
68071-3362-2 68071-3362 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68071-3362-2)
68071-3362-3 68071-3362 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3362-3)
68071-3362-4 68071-3362 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (68071-3362-4)
68071-3362-5 68071-3362 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68071-3362-5)
68071-3362-6 68071-3362 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-3362-6)
68071-3362-9 68071-3362 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-3362-9)
72189-324-30 72189-324 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20220221 N/A ANDA ANDA090796 Direct Rx IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-324-30)
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