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=ANDA213813"
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
70010-005-01 70010-005 HUMAN PRESCRIPTION DRUG DEXMETHYLPHENIDATE HYDROCHLORIDE DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 20201201 N/A ANDA ANDA213813 Granules Pharmaceuticals Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 10 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-005-01)
70010-009-01 70010-009 HUMAN PRESCRIPTION DRUG DEXMETHYLPHENIDATE HYDROCHLORIDE DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 20201201 N/A ANDA ANDA213813 Granules Pharmaceuticals Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 30 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-009-01)
70010-007-01 70010-007 HUMAN PRESCRIPTION DRUG DEXMETHYLPHENIDATE HYDROCHLORIDE DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 20201201 N/A ANDA ANDA213813 Granules Pharmaceuticals Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 20 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-007-01)
70010-011-01 70010-011 HUMAN PRESCRIPTION DRUG DEXMETHYLPHENIDATE HYDROCHLORIDE DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 20201201 N/A ANDA ANDA213813 Granules Pharmaceuticals Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 40 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-011-01)
70010-004-01 70010-004 HUMAN PRESCRIPTION DRUG DEXMETHYLPHENIDATE HYDROCHLORIDE DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 20201201 N/A ANDA ANDA213813 Granules Pharmaceuticals Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 5 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-004-01)
70010-008-01 70010-008 HUMAN PRESCRIPTION DRUG DEXMETHYLPHENIDATE HYDROCHLORIDE DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 20201201 N/A ANDA ANDA213813 Granules Pharmaceuticals Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 25 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-008-01)
70010-006-01 70010-006 HUMAN PRESCRIPTION DRUG DEXMETHYLPHENIDATE HYDROCHLORIDE DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 20201201 N/A ANDA ANDA213813 Granules Pharmaceuticals Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 15 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-006-01)
70010-010-01 70010-010 HUMAN PRESCRIPTION DRUG DEXMETHYLPHENIDATE HYDROCHLORIDE DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 20201201 N/A ANDA ANDA213813 Granules Pharmaceuticals Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 35 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-010-01)
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