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
70518-0904-0	70518-0904	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	lithium carbonate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20171212	20250630	ANDA	ANDA202288	REMEDYREPACK INC.	LITHIUM CARBONATE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-0904-0)
50090-6052-0	50090-6052	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	lithium carbonate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220823	N/A	ANDA	ANDA202288	A-S Medication Solutions	LITHIUM CARBONATE	300 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6052-0)
51079-180-20	51079-180	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	lithium carbonate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120810	N/A	ANDA	ANDA202288	Mylan Institutional Inc.	LITHIUM CARBONATE	300 mg/1	100 BLISTER PACK in 1 CARTON (51079-180-20) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-180-01)
0378-1300-01	0378-1300	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	lithium carbonate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120702	20250630	ANDA	ANDA202288	Mylan Pharmaceuticals Inc.	LITHIUM CARBONATE	300 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-1300-01)
0378-1300-05	0378-1300	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	lithium carbonate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120702	20250131	ANDA	ANDA202288	Mylan Pharmaceuticals Inc.	LITHIUM CARBONATE	300 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-1300-05)