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=ANDA202842"
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
72162-1488-1 72162-1488 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230330 N/A ANDA ANDA202842 Bryant Ranch Prepack DEXMETHYLPHENIDATE HYDROCHLORIDE 20 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1488-1)
72162-1473-1 72162-1473 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230330 N/A ANDA ANDA202842 Bryant Ranch Prepack DEXMETHYLPHENIDATE HYDROCHLORIDE 10 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1473-1)
72162-1507-1 72162-1507 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230330 N/A ANDA ANDA202842 Bryant Ranch Prepack DEXMETHYLPHENIDATE HYDROCHLORIDE 40 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1507-1)
72162-1472-1 72162-1472 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230330 N/A ANDA ANDA202842 Bryant Ranch Prepack DEXMETHYLPHENIDATE HYDROCHLORIDE 5 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1472-1)
72162-1496-1 72162-1496 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230330 N/A ANDA ANDA202842 Bryant Ranch Prepack DEXMETHYLPHENIDATE HYDROCHLORIDE 35 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1496-1)
72162-1493-1 72162-1493 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230330 N/A ANDA ANDA202842 Bryant Ranch Prepack DEXMETHYLPHENIDATE HYDROCHLORIDE 25 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1493-1)
49884-090-01 49884-090 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20170105 N/A ANDA ANDA202842 ENDO USA, Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 15 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-090-01)
49884-048-01 49884-048 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20170105 N/A ANDA ANDA202842 ENDO USA, Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 5 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-048-01)
49884-049-01 49884-049 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20170105 N/A ANDA ANDA202842 ENDO USA, Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 10 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-049-01)
49884-333-01 49884-333 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20170105 N/A ANDA ANDA202842 ENDO USA, Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 25 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-333-01)
49884-248-01 49884-248 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20170105 N/A ANDA ANDA202842 ENDO USA, Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 20 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-248-01)
49884-339-01 49884-339 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20170105 N/A ANDA ANDA202842 ENDO USA, Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 35 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-339-01)
49884-546-01 49884-546 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20170105 N/A ANDA ANDA202842 ENDO USA, Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 40 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-546-01)
49884-539-01 49884-539 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20170105 N/A ANDA ANDA202842 ENDO USA, Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 30 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-539-01)
63629-2174-1 63629-2174 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20211222 N/A ANDA ANDA202842 Bryant Ranch Prepack DEXMETHYLPHENIDATE HYDROCHLORIDE 25 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2174-1)
63629-2171-1 63629-2171 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20211222 N/A ANDA ANDA202842 Bryant Ranch Prepack DEXMETHYLPHENIDATE HYDROCHLORIDE 10 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2171-1)
63629-2173-1 63629-2173 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20211222 N/A ANDA ANDA202842 Bryant Ranch Prepack DEXMETHYLPHENIDATE HYDROCHLORIDE 20 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2173-1)
63629-2176-1 63629-2176 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20211222 N/A ANDA ANDA202842 Bryant Ranch Prepack DEXMETHYLPHENIDATE HYDROCHLORIDE 35 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2176-1)
63629-2177-1 63629-2177 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20211222 N/A ANDA ANDA202842 Bryant Ranch Prepack DEXMETHYLPHENIDATE HYDROCHLORIDE 40 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2177-1)
63629-2178-1 63629-2178 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Dexmethylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20211222 N/A ANDA ANDA202842 Bryant Ranch Prepack DEXMETHYLPHENIDATE HYDROCHLORIDE 5 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2178-1)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase