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=ANDA210139"
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
63629-1175-1 63629-1175 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride SOLUTION ORAL 20220726 N/A ANDA ANDA210139 Bryant Ranch Prepack METHYLPHENIDATE HYDROCHLORIDE 5 mg/5mL 500 mL in 1 BOTTLE (63629-1175-1)
63629-1176-1 63629-1176 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride SOLUTION ORAL 20210629 N/A ANDA ANDA210139 Bryant Ranch Prepack METHYLPHENIDATE HYDROCHLORIDE 10 mg/5mL 500 mL in 1 BOTTLE (63629-1176-1)
72162-1992-5 72162-1992 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride SOLUTION ORAL 20240403 N/A ANDA ANDA210139 Bryant Ranch Prepack METHYLPHENIDATE HYDROCHLORIDE 5 mg/5mL 500 mL in 1 BOTTLE (72162-1992-5)
72162-1993-5 72162-1993 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride SOLUTION ORAL 20240205 N/A ANDA ANDA210139 Bryant Ranch Prepack METHYLPHENIDATE HYDROCHLORIDE 10 mg/5mL 500 mL in 1 BOTTLE (72162-1993-5)
71930-024-52 71930-024 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride SOLUTION ORAL 20190329 N/A ANDA ANDA210139 Eywa Pharma Inc METHYLPHENIDATE HYDROCHLORIDE 5 mg/5mL 500 mL in 1 BOTTLE (71930-024-52)
71930-025-52 71930-025 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride SOLUTION ORAL 20190329 N/A ANDA ANDA210139 Eywa Pharma Inc METHYLPHENIDATE HYDROCHLORIDE 10 mg/5mL 500 mL in 1 BOTTLE (71930-025-52)
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