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
71205-238-30	71205-238	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate Extended-Release Tablet	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190301	N/A	NDA AUTHORIZED GENERIC	NDA018027	Proficient Rx LP	LITHIUM CARBONATE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-238-30)
71205-238-60	71205-238	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate Extended-Release Tablet	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190301	N/A	NDA AUTHORIZED GENERIC	NDA018027	Proficient Rx LP	LITHIUM CARBONATE	300 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-238-60)
71205-238-90	71205-238	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate Extended-Release Tablet	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190301	N/A	NDA AUTHORIZED GENERIC	NDA018027	Proficient Rx LP	LITHIUM CARBONATE	300 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-238-90)
62559-280-01	62559-280	HUMAN PRESCRIPTION DRUG	LITHOBID	lithium carbonate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140701	N/A	NDA	NDA018027	ANI Pharmaceuticals, Inc.	LITHIUM CARBONATE	300 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62559-280-01)