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=ANDA079031"
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
0093-5348-01 0093-5348 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride (LA) Methylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20120716 N/A ANDA ANDA079031 Teva Pharmaceuticals USA, Inc. METHYLPHENIDATE HYDROCHLORIDE 40 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5348-01)
0093-5347-01 0093-5347 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride (LA) Methylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20120716 N/A ANDA ANDA079031 Teva Pharmaceuticals USA, Inc. METHYLPHENIDATE HYDROCHLORIDE 30 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5347-01)
0093-5346-01 0093-5346 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride (LA) Methylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20120716 N/A ANDA ANDA079031 Teva Pharmaceuticals USA, Inc. METHYLPHENIDATE HYDROCHLORIDE 20 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5346-01)
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