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=ANDA078539"
符合检索条件的记录共 262 条，共 14 页，当前第 8 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
68071-3713-3 68071-3713 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET, FILM COATED ORAL 20241025 N/A ANDA ANDA078539 NuCare Pharmaceuticals, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3713-3)
68071-4705-4 68071-4705 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20190111 N/A ANDA ANDA078539 NuCare Pharmaceuticals,Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (68071-4705-4)
68071-3801-1 68071-3801 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET, FILM COATED ORAL 20250224 N/A ANDA ANDA078539 NuCare Pharmaceuticals, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (68071-3801-1)
68071-5047-3 68071-5047 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20190904 N/A ANDA ANDA078539 NuCare Pharmaceuticals,Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-5047-3)
68071-4328-4 68071-4328 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180312 N/A ANDA ANDA078539 NuCare Pharmceuticals,Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (68071-4328-4)
68071-4966-4 68071-4966 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA078539 NUCARE PHARMACEUTICALS INC ONDANSETRON HYDROCHLORIDE 8 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (68071-4966-4)
68071-4328-1 68071-4328 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180312 N/A ANDA ANDA078539 NuCare Pharmceuticals,Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (68071-4328-1)
68084-221-01 68084-221 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20230921 N/A ANDA ANDA078539 American Health Packaging ONDANSETRON HYDROCHLORIDE 8 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-221-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-221-11)
68084-220-01 68084-220 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20230921 N/A ANDA ANDA078539 American Health Packaging ONDANSETRON HYDROCHLORIDE 4 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-220-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-220-11)
68788-8582-6 68788-8582 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240212 N/A ANDA ANDA078539 Preferred Pharmaceuticals Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8582-6)
68788-8582-3 68788-8582 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240212 N/A ANDA ANDA078539 Preferred Pharmaceuticals Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8582-3)
68788-8582-5 68788-8582 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240212 N/A ANDA ANDA078539 Preferred Pharmaceuticals Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68788-8582-5)
68788-8582-2 68788-8582 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240212 N/A ANDA ANDA078539 Preferred Pharmaceuticals Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (68788-8582-2)
68788-8582-1 68788-8582 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240212 N/A ANDA ANDA078539 Preferred Pharmaceuticals Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (68788-8582-1)
68788-8651-3 68788-8651 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240429 N/A ANDA ANDA078539 Preferred Pharmaceuticals Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8651-3)
68788-8651-6 68788-8651 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240429 N/A ANDA ANDA078539 Preferred Pharmaceuticals Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8651-6)
68788-8651-1 68788-8651 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240429 N/A ANDA ANDA078539 Preferred Pharmaceuticals Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (68788-8651-1)
68788-8651-5 68788-8651 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240429 N/A ANDA ANDA078539 Preferred Pharmaceuticals Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68788-8651-5)
68788-8651-2 68788-8651 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240429 N/A ANDA ANDA078539 Preferred Pharmaceuticals Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (68788-8651-2)
68788-9368-1 68788-9368 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20120612 N/A ANDA ANDA078539 Preferred Pharmaceuticals, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (68788-9368-1)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase