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=ANDA078873"
符合检索条件的记录共 3 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
0093-5298-01 0093-5298 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride (CD) Methylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20120927 20241031 ANDA ANDA078873 Teva Pharmaceuticals USA, Inc. METHYLPHENIDATE HYDROCHLORIDE 40 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5298-01)
0093-5293-01 0093-5293 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride (CD) Methylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20120927 20241031 ANDA ANDA078873 Teva Pharmaceuticals USA, Inc. METHYLPHENIDATE HYDROCHLORIDE 60 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5293-01)
0093-5292-01 0093-5292 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride (CD) Methylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20120927 20241031 ANDA ANDA078873 Teva Pharmaceuticals USA, Inc. METHYLPHENIDATE HYDROCHLORIDE 50 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5292-01)
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