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=ANDA078458"
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
51862-614-30 51862-614 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride (LA) Methylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20181206 N/A ANDA ANDA078458 Mayne Pharma METHYLPHENIDATE HYDROCHLORIDE 60 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51862-614-30)
51862-612-01 51862-612 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride (LA) Methylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20190610 N/A ANDA ANDA078458 Mayne Pharma METHYLPHENIDATE HYDROCHLORIDE 40 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51862-612-01)
51862-611-01 51862-611 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride (LA) Methylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20190610 N/A ANDA ANDA078458 Mayne Pharma METHYLPHENIDATE HYDROCHLORIDE 30 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51862-611-01)
51862-610-01 51862-610 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride (LA) Methylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20190610 N/A ANDA ANDA078458 Mayne Pharma METHYLPHENIDATE HYDROCHLORIDE 20 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51862-610-01)
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