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=ANDA211796"
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
70010-014-01 70010-014 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20190910 N/A ANDA ANDA211796 Granules Pharmaceuticals Inc. METHYLPHENIDATE HYDROCHLORIDE 30 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-014-01)
70010-015-01 70010-015 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20190910 N/A ANDA ANDA211796 Granules Pharmaceuticals Inc. METHYLPHENIDATE HYDROCHLORIDE 40 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-015-01)
70010-013-01 70010-013 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20190910 N/A ANDA ANDA211796 Granules Pharmaceuticals Inc. METHYLPHENIDATE HYDROCHLORIDE 20 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-013-01)
70010-012-01 70010-012 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20190910 N/A ANDA ANDA211796 Granules Pharmaceuticals Inc. METHYLPHENIDATE HYDROCHLORIDE 10 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-012-01)
70010-016-03 70010-016 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20190910 N/A ANDA ANDA211796 Granules Pharmaceuticals Inc. METHYLPHENIDATE HYDROCHLORIDE 60 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-016-03)
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