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）

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
63629-9469-1	63629-9469	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20221128	N/A	ANDA	ANDA212631	Bryant Ranch Prepack	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (63629-9469-1)
63629-9468-1	63629-9468	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20221117	N/A	ANDA	ANDA212631	Bryant Ranch Prepack	DEXMETHYLPHENIDATE HYDROCHLORIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (63629-9468-1)
63629-9467-1	63629-9467	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20221117	N/A	ANDA	ANDA212631	Bryant Ranch Prepack	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (63629-9467-1)
67877-655-01	67877-655	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20190721	N/A	ANDA	ANDA212631	Ascend Laboratories, LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (67877-655-01)
67877-656-05	67877-656	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20190721	N/A	ANDA	ANDA212631	Ascend Laboratories, LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	500 TABLET in 1 BOTTLE (67877-656-05)
67877-656-30	67877-656	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20190721	N/A	ANDA	ANDA212631	Ascend Laboratories, LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	30 TABLET in 1 BOTTLE (67877-656-30)
67877-657-01	67877-657	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20190721	N/A	ANDA	ANDA212631	Ascend Laboratories, LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (67877-657-01)
67877-657-05	67877-657	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20190721	N/A	ANDA	ANDA212631	Ascend Laboratories, LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	500 TABLET in 1 BOTTLE (67877-657-05)
67877-657-30	67877-657	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20190721	N/A	ANDA	ANDA212631	Ascend Laboratories, LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	30 TABLET in 1 BOTTLE (67877-657-30)
67877-655-05	67877-655	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20190721	N/A	ANDA	ANDA212631	Ascend Laboratories, LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	2.5 mg/1	500 TABLET in 1 BOTTLE (67877-655-05)
67877-655-30	67877-655	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20190721	N/A	ANDA	ANDA212631	Ascend Laboratories, LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	2.5 mg/1	30 TABLET in 1 BOTTLE (67877-655-30)
67877-656-01	67877-656	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20190721	N/A	ANDA	ANDA212631	Ascend Laboratories, LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (67877-656-01)