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=ANDA205825"
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
65162-783-03 65162-783 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20171222 N/A ANDA ANDA205825 Amneal Pharmaceuticals LLC MEMANTINE HYDROCHLORIDE 14 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-783-03)
65162-783-09 65162-783 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20171222 N/A ANDA ANDA205825 Amneal Pharmaceuticals LLC MEMANTINE HYDROCHLORIDE 14 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-783-09)
65162-783-50 65162-783 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20171222 N/A ANDA ANDA205825 Amneal Pharmaceuticals LLC MEMANTINE HYDROCHLORIDE 14 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-783-50)
65162-782-03 65162-782 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20171222 N/A ANDA ANDA205825 Amneal Pharmaceuticals LLC MEMANTINE HYDROCHLORIDE 7 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-782-03)
65162-782-09 65162-782 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20171222 N/A ANDA ANDA205825 Amneal Pharmaceuticals LLC MEMANTINE HYDROCHLORIDE 7 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-782-09)
65162-782-50 65162-782 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20171222 N/A ANDA ANDA205825 Amneal Pharmaceuticals LLC MEMANTINE HYDROCHLORIDE 7 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-782-50)
65162-785-03 65162-785 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20171222 N/A ANDA ANDA205825 Amneal Pharmaceuticals LLC MEMANTINE HYDROCHLORIDE 28 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-785-03)
65162-785-09 65162-785 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20171222 N/A ANDA ANDA205825 Amneal Pharmaceuticals LLC MEMANTINE HYDROCHLORIDE 28 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-785-09)
65162-785-50 65162-785 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20171222 N/A ANDA ANDA205825 Amneal Pharmaceuticals LLC MEMANTINE HYDROCHLORIDE 28 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-785-50)
65162-784-03 65162-784 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20171222 N/A ANDA ANDA205825 Amneal Pharmaceuticals LLC MEMANTINE HYDROCHLORIDE 21 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-784-03)
65162-784-09 65162-784 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20171222 N/A ANDA ANDA205825 Amneal Pharmaceuticals LLC MEMANTINE HYDROCHLORIDE 21 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-784-09)
65162-784-50 65162-784 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20171222 N/A ANDA ANDA205825 Amneal Pharmaceuticals LLC MEMANTINE HYDROCHLORIDE 21 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-784-50)
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