美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=DEXMETHYLPHENIDATE HYDROCHLORIDE"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
DEXMETHYLPHENIDATE HYDROCHLORIDE 202842 007 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 35MG No No 2016/11/30 2016/11/30 ENDO OPERATIONS Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 202842 008 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 40MG No No 2016/11/30 2016/11/30 ENDO OPERATIONS Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 202731 001 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 25MG No No 2017/07/05 2017/07/05 TEVA PHARMS USA Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 202731 002 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 40MG No No 2017/07/05 2013/11/19 TEVA PHARMS USA Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 202731 003 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 30MG No No 2017/07/05 2014/05/19 TEVA PHARMS USA Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 202731 004 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 35MG No No 2017/07/05 2017/07/05 TEVA PHARMS USA Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 202731 005 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 30MG No No 2017/07/05 -- TEVA PHARMS USA Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 203614 001 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 25MG No No 2017/07/05 2017/07/05 IMPAX LABS INC Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 203614 002 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 35MG No No 2017/07/05 2017/07/05 IMPAX LABS INC Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 209468 001 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 2.5MG No No 2017/09/25 2017/09/25 LANNETT CO INC Discontinued
DEXMETHYLPHENIDATE HYDROCHLORIDE 209468 002 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 5MG No No 2017/09/25 2017/09/25 LANNETT CO INC Discontinued
DEXMETHYLPHENIDATE HYDROCHLORIDE 209468 003 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 10MG No No 2017/09/25 2017/09/25 LANNETT CO INC Discontinued
DEXMETHYLPHENIDATE HYDROCHLORIDE 208756 001 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 2.5MG No No 2017/11/20 2017/11/20 RHODES PHARMS Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 208756 002 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 5MG No No 2017/11/20 2017/11/20 RHODES PHARMS Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 208756 003 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 10MG No No 2017/11/20 2017/11/20 RHODES PHARMS Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 209211 001 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 5MG No No 2018/09/19 2018/09/19 CEDIPROF INC Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 209211 002 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 10MG No No 2018/09/19 2018/09/19 CEDIPROF INC Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 210279 001 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 5MG No No 2018/10/09 2018/10/09 ADARE PHARMS INC Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 210279 002 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 10MG No No 2018/10/09 2018/10/09 ADARE PHARMS INC Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 210279 003 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 15MG No No 2018/10/09 2018/10/09 ADARE PHARMS INC Prescription
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