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=ANDA211009"
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
50268-548-12 50268-548 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20210422 N/A ANDA ANDA211009 AvPAK METHYLPHENIDATE HYDROCHLORIDE 54 mg/1 20 BLISTER PACK in 1 BOX (50268-548-12) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-548-11)
50268-547-12 50268-547 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20210422 N/A ANDA ANDA211009 AvPAK METHYLPHENIDATE HYDROCHLORIDE 36 mg/1 20 BLISTER PACK in 1 BOX (50268-547-12) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-547-11)
50268-546-12 50268-546 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20210422 N/A ANDA ANDA211009 AvPAK METHYLPHENIDATE HYDROCHLORIDE 27 mg/1 20 BLISTER PACK in 1 BOX (50268-546-12) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-546-11)
60687-554-21 60687-554 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20200625 N/A ANDA ANDA211009 American Health Packaging METHYLPHENIDATE HYDROCHLORIDE 36 mg/1 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-554-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-554-11)
60687-565-21 60687-565 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20240922 N/A ANDA ANDA211009 American Health Packaging METHYLPHENIDATE HYDROCHLORIDE 54 mg/1 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-565-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-565-11)
50268-545-12 50268-545 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20210422 N/A ANDA ANDA211009 AvPAK METHYLPHENIDATE HYDROCHLORIDE 18 mg/1 20 BLISTER PACK in 1 BOX (50268-545-12) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-545-11)
60687-532-21 60687-532 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20200625 N/A ANDA ANDA211009 American Health Packaging METHYLPHENIDATE HYDROCHLORIDE 18 mg/1 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-532-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-532-11)
60687-543-21 60687-543 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20200625 N/A ANDA ANDA211009 American Health Packaging METHYLPHENIDATE HYDROCHLORIDE 27 mg/1 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-543-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-543-11)
72865-135-01 72865-135 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20200224 N/A ANDA ANDA211009 XLCare Pharmaceuticals, Inc. METHYLPHENIDATE HYDROCHLORIDE 36 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-135-01)
72865-136-01 72865-136 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20200224 N/A ANDA ANDA211009 XLCare Pharmaceuticals, Inc. METHYLPHENIDATE HYDROCHLORIDE 54 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-136-01)
72865-133-01 72865-133 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20200224 N/A ANDA ANDA211009 XLCare Pharmaceuticals, Inc. METHYLPHENIDATE HYDROCHLORIDE 18 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-133-01)
72865-134-01 72865-134 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20200224 N/A ANDA ANDA211009 XLCare Pharmaceuticals, Inc. METHYLPHENIDATE HYDROCHLORIDE 27 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-134-01)
31722-952-01 31722-952 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20190903 N/A ANDA ANDA211009 Camber Pharmaceuticals, Inc. METHYLPHENIDATE HYDROCHLORIDE 18 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-952-01)
31722-953-01 31722-953 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20190903 N/A ANDA ANDA211009 Camber Pharmaceuticals, Inc. METHYLPHENIDATE HYDROCHLORIDE 27 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-953-01)
31722-954-01 31722-954 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20190903 N/A ANDA ANDA211009 Camber Pharmaceuticals, Inc. METHYLPHENIDATE HYDROCHLORIDE 36 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-954-01)
31722-955-01 31722-955 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20190903 N/A ANDA ANDA211009 Camber Pharmaceuticals, Inc. METHYLPHENIDATE HYDROCHLORIDE 54 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-955-01)
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