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=ANDA217038"
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
68071-3591-4 68071-3591 HUMAN PRESCRIPTION DRUG ketorolac tromethamine ketorolac tromethamine TABLET, FILM COATED ORAL 20240405 N/A ANDA ANDA217038 NuCare Pharmaceuticals,Inc. KETOROLAC TROMETHAMINE 10 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (68071-3591-4)
68071-2983-2 68071-2983 HUMAN PRESCRIPTION DRUG ketorolac tromethamine ketorolac tromethamine TABLET, FILM COATED ORAL 20230619 N/A ANDA ANDA217038 NuCare Pharmaceuticals,Inc. KETOROLAC TROMETHAMINE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68071-2983-2)
70771-1747-1 70771-1747 HUMAN PRESCRIPTION DRUG ketorolac tromethamine ketorolac tromethamine TABLET, FILM COATED ORAL 20221110 N/A ANDA ANDA217038 Zydus Lifesciences Limited KETOROLAC TROMETHAMINE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1747-1)
70710-1710-1 70710-1710 HUMAN PRESCRIPTION DRUG ketorolac tromethamine ketorolac tromethamine TABLET, FILM COATED ORAL 20221110 N/A ANDA ANDA217038 Zydus Pharmaceuticals (USA) Inc. KETOROLAC TROMETHAMINE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1710-1)
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