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=ANDA076255"
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
43598-165-78 43598-165 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET, FILM COATED ORAL 20131210 N/A ANDA ANDA076255 Dr. Reddy's Laboratories Inc. OLANZAPINE 7.5 mg/1 10 BLISTER PACK in 1 CARTON (43598-165-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-165-79)
43598-165-01 43598-165 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET, FILM COATED ORAL 20131210 N/A ANDA ANDA076255 Dr. Reddy's Laboratories Inc. OLANZAPINE 7.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (43598-165-01)
68084-740-01 68084-740 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET, FILM COATED ORAL 20140522 N/A ANDA ANDA076255 American Health Packaging OLANZAPINE 10 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-740-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-740-11)
68788-8722-3 68788-8722 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET, FILM COATED ORAL 20240809 N/A ANDA ANDA076255 Preferred Pharmaceuticals Inc. OLANZAPINE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8722-3)
68788-8722-6 68788-8722 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET, FILM COATED ORAL 20240809 N/A ANDA ANDA076255 Preferred Pharmaceuticals Inc. OLANZAPINE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8722-6)
68788-8722-9 68788-8722 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET, FILM COATED ORAL 20240809 N/A ANDA ANDA076255 Preferred Pharmaceuticals Inc. OLANZAPINE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8722-9)
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