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=ANDA078329"
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
68788-8531-4 68788-8531 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20231006 N/A ANDA ANDA078329 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (68788-8531-4)
68788-8531-5 68788-8531 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20231006 N/A ANDA ANDA078329 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (68788-8531-5)
68788-8531-6 68788-8531 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20231006 N/A ANDA ANDA078329 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8531-6)
68788-8531-7 68788-8531 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20231006 N/A ANDA ANDA078329 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (68788-8531-7)
68788-8531-8 68788-8531 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20231006 N/A ANDA ANDA078329 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (68788-8531-8)
68788-8531-9 68788-8531 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20231006 N/A ANDA ANDA078329 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8531-9)
68788-8710-1 68788-8710 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240705 N/A ANDA ANDA078329 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-8710-1)
68788-8710-2 68788-8710 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240705 N/A ANDA ANDA078329 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68788-8710-2)
68788-8710-3 68788-8710 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240705 N/A ANDA ANDA078329 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8710-3)
68788-8710-4 68788-8710 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240705 N/A ANDA ANDA078329 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (68788-8710-4)
68788-8710-5 68788-8710 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240705 N/A ANDA ANDA078329 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (68788-8710-5)
68788-8710-6 68788-8710 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240705 N/A ANDA ANDA078329 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8710-6)
68788-8710-7 68788-8710 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240705 N/A ANDA ANDA078329 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (68788-8710-7)
68788-8710-8 68788-8710 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240705 N/A ANDA ANDA078329 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (68788-8710-8)
68788-8710-9 68788-8710 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240705 N/A ANDA ANDA078329 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8710-9)
70512-780-10 70512-780 HUMAN PRESCRIPTION DRUG Ibuprofen ibuprofen TABLET ORAL 20241201 N/A ANDA ANDA078329 SOLA Pharmaceuticals, LLC IBUPROFEN 800 mg/1 100 TABLET in 1 BOTTLE (70512-780-10)
70512-780-50 70512-780 HUMAN PRESCRIPTION DRUG Ibuprofen ibuprofen TABLET ORAL 20241201 N/A ANDA ANDA078329 SOLA Pharmaceuticals, LLC IBUPROFEN 800 mg/1 500 TABLET in 1 BOTTLE (70512-780-50)
80425-0537-1 80425-0537 HUMAN PRESCRIPTION DRUG Ibuprofen ibuprofen TABLET ORAL 20250805 N/A ANDA ANDA078329 Advanced Rx of Tennessee, LLC IBUPROFEN 800 mg/1 30 TABLET in 1 BOTTLE (80425-0537-1)
80425-0537-2 80425-0537 HUMAN PRESCRIPTION DRUG Ibuprofen ibuprofen TABLET ORAL 20250805 N/A ANDA ANDA078329 Advanced Rx of Tennessee, LLC IBUPROFEN 800 mg/1 60 TABLET in 1 BOTTLE (80425-0537-2)
80425-0537-3 80425-0537 HUMAN PRESCRIPTION DRUG Ibuprofen ibuprofen TABLET ORAL 20250805 N/A ANDA ANDA078329 Advanced Rx of Tennessee, LLC IBUPROFEN 800 mg/1 90 TABLET in 1 BOTTLE (80425-0537-3)
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