美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=METHYLPHENIDATE"
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 078992 004 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 30MG No No 2021/11/23 2013/11/18 MEDICAP LABS Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 078992 005 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 20MG No No 2021/11/23 2021/11/23 MEDICAP LABS Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 078992 006 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 40MG No No 2021/11/23 2021/11/23 MEDICAP LABS Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 215523 001 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 5MG No No 2021/12/08 2021/12/08 ASCENT PHARMS INC Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 215523 002 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 10MG No No 2021/12/08 2021/12/08 ASCENT PHARMS INC Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 215523 003 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 15MG No No 2021/12/08 2021/12/08 ASCENT PHARMS INC Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 215523 004 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 20MG No No 2021/12/08 2021/12/08 ASCENT PHARMS INC Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 215523 005 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 25MG No No 2021/12/08 2021/12/08 ASCENT PHARMS INC Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 215523 006 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 30MG No No 2021/12/08 2021/12/08 ASCENT PHARMS INC Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 215523 007 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 35MG No No 2021/12/08 2021/12/08 ASCENT PHARMS INC Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 215523 008 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 40MG No No 2021/12/08 2021/12/08 ASCENT PHARMS INC Prescription
METHYLPHENIDATE 206497 001 ANDA METHYLPHENIDATE FILM, EXTENDED RELEASE;TRANSDERMAL 10MG/9HR (1.1MG/HR) No No 2022/03/14 2022/03/14 MYLAN TECH VIATRIS Prescription
METHYLPHENIDATE 206497 002 ANDA METHYLPHENIDATE FILM, EXTENDED RELEASE;TRANSDERMAL 15MG/9HR (1.6MG/HR) No No 2022/03/14 2022/03/14 MYLAN TECH VIATRIS Prescription
METHYLPHENIDATE 206497 003 ANDA METHYLPHENIDATE FILM, EXTENDED RELEASE;TRANSDERMAL 20MG/9HR (2.2MG/HR) No No 2022/03/14 2022/03/14 MYLAN TECH VIATRIS Prescription
METHYLPHENIDATE 206497 004 ANDA METHYLPHENIDATE FILM, EXTENDED RELEASE;TRANSDERMAL 30MG/9HR (3.3MG/HR) No No 2022/03/14 2022/03/14 MYLAN TECH VIATRIS Prescription
METHYLPHENIDATE HYDROCHLORIDE 214111 001 ANDA METHYLPHENIDATE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 18MG No No 2022/05/31 2022/05/31 RHODES PHARMS Discontinued
METHYLPHENIDATE HYDROCHLORIDE 214111 002 ANDA METHYLPHENIDATE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 27MG No No 2022/05/31 2022/05/31 RHODES PHARMS Discontinued
METHYLPHENIDATE HYDROCHLORIDE 214111 003 ANDA METHYLPHENIDATE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 36MG No No 2022/05/31 2022/05/31 RHODES PHARMS Discontinued
METHYLPHENIDATE HYDROCHLORIDE 214111 004 ANDA METHYLPHENIDATE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 54MG No No 2022/05/31 2022/05/31 RHODES PHARMS Discontinued
METHYLPHENIDATE HYDROCHLORIDE 214202 001 ANDA METHYLPHENIDATE HYDROCHLORIDE TABLET, EXTENDED RELEASE, CHEWABLE;ORAL 20MG No No 2023/02/07 (TA) -- TEVA PHARMS USA None (Tentative Approval)
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