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）

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
70436-056-04	70436-056	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	memantine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20211115	N/A	ANDA	ANDA211100	Slate Run Pharmaceuticals, LLC	MEMANTINE HYDROCHLORIDE	21 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70436-056-04)
70436-057-04	70436-057	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	memantine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20211115	N/A	ANDA	ANDA211100	Slate Run Pharmaceuticals, LLC	MEMANTINE HYDROCHLORIDE	28 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70436-057-04)
70436-057-06	70436-057	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	memantine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20211115	N/A	ANDA	ANDA211100	Slate Run Pharmaceuticals, LLC	MEMANTINE HYDROCHLORIDE	28 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70436-057-06)
70436-055-06	70436-055	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	memantine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20211115	N/A	ANDA	ANDA211100	Slate Run Pharmaceuticals, LLC	MEMANTINE HYDROCHLORIDE	14 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70436-055-06)
70436-055-04	70436-055	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	memantine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20211115	N/A	ANDA	ANDA211100	Slate Run Pharmaceuticals, LLC	MEMANTINE HYDROCHLORIDE	14 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70436-055-04)
70436-054-04	70436-054	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	memantine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20211115	N/A	ANDA	ANDA211100	Slate Run Pharmaceuticals, LLC	MEMANTINE HYDROCHLORIDE	7 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70436-054-04)