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
62756-430-88	62756-430	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate	TABLET	ORAL	20100708	N/A	ANDA	ANDA091027	Sun Pharmaceutical Industries, Inc.	LITHIUM CARBONATE	300 mg/1	100 TABLET in 1 BOTTLE (62756-430-88)
70518-2699-0	70518-2699	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate	TABLET	ORAL	20200420	N/A	ANDA	ANDA091027	REMEDYREPACK INC.	LITHIUM CARBONATE	300 mg/1	30 TABLET in 1 BLISTER PACK (70518-2699-0)
62756-430-83	62756-430	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate	TABLET	ORAL	20100708	N/A	ANDA	ANDA091027	Sun Pharmaceutical Industries, Inc.	LITHIUM CARBONATE	300 mg/1	30 TABLET in 1 BOTTLE (62756-430-83)
62756-430-18	62756-430	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate	TABLET	ORAL	20100708	N/A	ANDA	ANDA091027	Sun Pharmaceutical Industries, Inc.	LITHIUM CARBONATE	300 mg/1	1000 TABLET in 1 BOTTLE (62756-430-18)
62756-430-08	62756-430	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate	TABLET	ORAL	20100708	N/A	ANDA	ANDA091027	Sun Pharmaceutical Industries, Inc.	LITHIUM CARBONATE	300 mg/1	100 TABLET in 1 BOTTLE (62756-430-08)