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
68071-4459-6 68071-4459 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20180531 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (68071-4459-6)
68071-5135-0 68071-5135 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191216 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68071-5135-0)
70518-2432-1 70518-2432 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210526 N/A ANDA ANDA090796 REMEDYREPACK INC. IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2432-1)
49483-604-01 49483-604 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 TIME CAP LABORATORIES, INC IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (49483-604-01)
49483-604-03 49483-604 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 TIME CAP LABORATORIES, INC IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (49483-604-03)
49483-604-05 49483-604 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 TIME CAP LABORATORIES, INC IBUPROFEN 800 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (49483-604-05)
49483-604-50 49483-604 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 TIME CAP LABORATORIES, INC IBUPROFEN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (49483-604-50)
51655-275-20 51655-275 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210709 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 800 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-20)
51655-275-21 51655-275 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20201029 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 800 mg/1 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-21)
68071-5134-6 68071-5134 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191213 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 400 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (68071-5134-6)
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)
71335-1396-4 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (71335-1396-4)
71335-1396-5 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1396-5)
71335-1396-6 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1396-6)
71335-1396-7 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-1396-7)
68071-5126-3 68071-5126 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191211 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-5126-3)
68071-5126-9 68071-5126 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191211 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-5126-9)
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