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
METHYLPHENIDATE HYDROCHLORIDE 211009 004 ANDA METHYLPHENIDATE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 54MG No No 2019/09/03 2019/09/03 ASCENT PHARMS INC Prescription
METHYLPHENIDATE HYDROCHLORIDE 211779 001 ANDA METHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 5MG No No 2019/10/04 2019/10/04 ALKEM LABS LTD Prescription
METHYLPHENIDATE HYDROCHLORIDE 211779 002 ANDA METHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 10MG No No 2019/10/04 2019/10/04 ALKEM LABS LTD Prescription
METHYLPHENIDATE HYDROCHLORIDE 211779 003 ANDA METHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 20MG No No 2019/10/04 2019/10/04 ALKEM LABS LTD Prescription
DEXMETHYLPHENIDATE HYDROCHLORIDE 209754 001 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 5MG No No 2020/03/24 2020/03/24 BIONPHARMA Discontinued
DEXMETHYLPHENIDATE HYDROCHLORIDE 209754 002 ANDA DEXMETHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 10MG No No 2020/03/24 2020/03/24 BIONPHARMA Discontinued
METHYLPHENIDATE HYDROCHLORIDE 211647 001 ANDA METHYLPHENIDATE HYDROCHLORIDE SOLUTION;ORAL 5MG/5ML No No 2020/03/30 2020/03/30 ALKEM LABS LTD Prescription
METHYLPHENIDATE HYDROCHLORIDE 211647 002 ANDA METHYLPHENIDATE HYDROCHLORIDE SOLUTION;ORAL 10MG/5ML No No 2020/03/30 2020/03/30 ALKEM LABS LTD Prescription
METHYLPHENIDATE HYDROCHLORIDE 210764 001 ANDA METHYLPHENIDATE HYDROCHLORIDE SOLUTION;ORAL 5MG/5ML No No 2020/04/10 2020/04/10 ANDA REPOSITORY Prescription
METHYLPHENIDATE HYDROCHLORIDE 210764 002 ANDA METHYLPHENIDATE HYDROCHLORIDE SOLUTION;ORAL 10MG/5ML No No 2020/04/10 2020/04/10 ANDA REPOSITORY Prescription
METHYLPHENIDATE HYDROCHLORIDE 213567 001 ANDA METHYLPHENIDATE HYDROCHLORIDE SOLUTION;ORAL 5MG/5ML No No 2020/06/04 2020/06/04 QUAGEN Prescription
METHYLPHENIDATE HYDROCHLORIDE 213567 002 ANDA METHYLPHENIDATE HYDROCHLORIDE SOLUTION;ORAL 10MG/5ML No No 2020/06/04 2020/06/04 QUAGEN Prescription
METHYLPHENIDATE 210924 001 ANDA METHYLPHENIDATE TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE;ORAL 8.6MG No No 2020/06/19 2020/06/19 ACTAVIS ELIZABETH Discontinued
METHYLPHENIDATE 210924 002 ANDA METHYLPHENIDATE TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE;ORAL 17.3MG No No 2020/06/19 2020/06/19 ACTAVIS ELIZABETH Discontinued
METHYLPHENIDATE 210924 003 ANDA METHYLPHENIDATE TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE;ORAL 25.9MG No No 2020/06/19 2020/06/19 ACTAVIS ELIZABETH Discontinued
METHYLPHENIDATE HYDROCHLORIDE 212697 001 ANDA METHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 5MG No No 2020/07/23 2020/07/23 PRINSTON INC Prescription
METHYLPHENIDATE HYDROCHLORIDE 212697 002 ANDA METHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 10MG No No 2020/07/23 2020/07/23 PRINSTON INC Prescription
METHYLPHENIDATE HYDROCHLORIDE 212697 003 ANDA METHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 20MG No No 2020/07/23 2020/07/23 PRINSTON INC Prescription
METHYLPHENIDATE HYDROCHLORIDE 213473 001 ANDA METHYLPHENIDATE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 18MG No No 2020/07/29 2020/07/29 GRANULES Prescription
METHYLPHENIDATE HYDROCHLORIDE 213473 002 ANDA METHYLPHENIDATE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 27MG No No 2020/07/29 2020/07/29 GRANULES Prescription
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