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=NDA021121"
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
50458-588-01 50458-588 HUMAN PRESCRIPTION DRUG CONCERTA Methylphenidate hydrochloride TABLET, EXTENDED RELEASE ORAL 20000801 N/A NDA NDA021121 Janssen Pharmaceuticals, Inc. METHYLPHENIDATE HYDROCHLORIDE 27 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50458-588-01)
50458-585-01 50458-585 HUMAN PRESCRIPTION DRUG CONCERTA Methylphenidate hydrochloride TABLET, EXTENDED RELEASE ORAL 20000801 N/A NDA NDA021121 Janssen Pharmaceuticals, Inc. METHYLPHENIDATE HYDROCHLORIDE 18 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50458-585-01)
50458-586-01 50458-586 HUMAN PRESCRIPTION DRUG CONCERTA Methylphenidate hydrochloride TABLET, EXTENDED RELEASE ORAL 20000801 N/A NDA NDA021121 Janssen Pharmaceuticals, Inc. METHYLPHENIDATE HYDROCHLORIDE 36 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50458-586-01)
50458-587-01 50458-587 HUMAN PRESCRIPTION DRUG CONCERTA Methylphenidate hydrochloride TABLET, EXTENDED RELEASE ORAL 20000801 N/A NDA NDA021121 Janssen Pharmaceuticals, Inc. METHYLPHENIDATE HYDROCHLORIDE 54 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50458-587-01)
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