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
63187-451-90 63187-451 HUMAN PRESCRIPTION DRUG ibuprofen ibuprofen TABLET ORAL 20190101 N/A ANDA ANDA090796 Proficient Rx LP IBUPROFEN 600 mg/1 90 TABLET in 1 BOTTLE (63187-451-90)
80425-0243-4 80425-0243 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230110 N/A ANDA ANDA090796 Advanced Rx Pharmacy of Tennessee, LLC IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (80425-0243-4)
68071-5140-3 68071-5140 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191231 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (68071-5140-3)
68071-5140-6 68071-5140 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200106 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (68071-5140-6)
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)
43063-867-60 43063-867 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20180705 N/A ANDA ANDA090796 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-60)
43063-936-30 43063-936 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20190214 N/A ANDA ANDA090796 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-936-30)
68071-4243-1 68071-4243 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20180122 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68071-4243-1)
71335-1396-0 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 84 TABLET, FILM COATED in 1 BOTTLE (71335-1396-0)
71335-1396-1 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-1396-1)
71335-1396-2 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-1396-2)
71335-1396-3 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71335-1396-3)
53002-3981-3 53002-3981 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210101 N/A ANDA ANDA090796 RPK Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (53002-3981-3)
53002-3981-5 53002-3981 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210101 N/A ANDA ANDA090796 RPK Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (53002-3981-5)
45865-945-30 45865-945 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20181212 N/A ANDA ANDA090796 medsource pharmaceuticals IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (45865-945-30)
45865-945-60 45865-945 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20181212 N/A ANDA ANDA090796 medsource pharmaceuticals IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (45865-945-60)
80425-0132-1 80425-0132 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 Advanced Rx Pharmacy of Tennessee, LLC IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0132-1)
80425-0132-2 80425-0132 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 Advanced Rx Pharmacy of Tennessee, LLC IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0132-2)
80425-0132-3 80425-0132 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 Advanced Rx Pharmacy of Tennessee, LLC IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (80425-0132-3)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase