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
70518-4115-0	70518-4115	HUMAN PRESCRIPTION DRUG	Lithium carbonate	Lithium carbonate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240627	N/A	ANDA	ANDA205532	REMEDYREPACK INC.	LITHIUM CARBONATE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4115-0)
23155-763-01	23155-763	HUMAN PRESCRIPTION DRUG	Lithium carbonate	Lithium carbonate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201020	N/A	ANDA	ANDA205532	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	LITHIUM CARBONATE	300 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155-763-01)
23155-763-05	23155-763	HUMAN PRESCRIPTION DRUG	Lithium carbonate	Lithium carbonate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201020	N/A	ANDA	ANDA205532	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	LITHIUM CARBONATE	300 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155-763-05)