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
50090-1470-0	50090-1470	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141128	N/A	ANDA	ANDA091544	A-S Medication Solutions	LITHIUM CARBONATE	300 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-1470-0)
67046-1575-3	67046-1575	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250904	N/A	ANDA	ANDA091544	Coupler LLC	LITHIUM CARBONATE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (67046-1575-3)
68462-223-01	68462-223	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20101227	N/A	ANDA	ANDA091544	Glenmark Pharmaceuticals Inc., USA	LITHIUM CARBONATE	300 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-223-01)