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=ANDA210279"
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
0527-8106-37 0527-8106 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Extended-Release dexmethylphenidate hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20181009 N/A ANDA ANDA210279 Lannett Company, Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 5 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-8106-37)
0527-8110-37 0527-8110 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Extended-Release dexmethylphenidate hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20181009 N/A ANDA ANDA210279 Lannett Company, Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 25 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-8110-37)
0527-8108-37 0527-8108 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Extended-Release dexmethylphenidate hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20181009 N/A ANDA ANDA210279 Lannett Company, Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 15 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-8108-37)
0527-8112-37 0527-8112 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Extended-Release dexmethylphenidate hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20181009 N/A ANDA ANDA210279 Lannett Company, Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 35 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-8112-37)
0527-8109-37 0527-8109 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Extended-Release dexmethylphenidate hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20181009 N/A ANDA ANDA210279 Lannett Company, Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 20 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-8109-37)
0527-8113-37 0527-8113 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Extended-Release dexmethylphenidate hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20181009 N/A ANDA ANDA210279 Lannett Company, Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 40 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-8113-37)
0527-8107-37 0527-8107 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Extended-Release dexmethylphenidate hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20181009 N/A ANDA ANDA210279 Lannett Company, Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 10 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-8107-37)
0527-8111-37 0527-8111 HUMAN PRESCRIPTION DRUG Dexmethylphenidate Hydrochloride Extended-Release dexmethylphenidate hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20181009 N/A ANDA ANDA210279 Lannett Company, Inc. DEXMETHYLPHENIDATE HYDROCHLORIDE 30 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-8111-37)
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