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
72789-171-82	72789-171	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate	TABLET, EXTENDED RELEASE	ORAL	20230823	N/A	ANDA	ANDA076832	PD-Rx Pharmaceuticals, Inc.	LITHIUM CARBONATE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-171-82)
72789-171-30	72789-171	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate	TABLET, EXTENDED RELEASE	ORAL	20210104	N/A	ANDA	ANDA076832	PD-Rx Pharmaceuticals, Inc.	LITHIUM CARBONATE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-171-30)
72789-171-01	72789-171	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate	TABLET, EXTENDED RELEASE	ORAL	20230728	N/A	ANDA	ANDA076832	PD-Rx Pharmaceuticals, Inc.	LITHIUM CARBONATE	300 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-171-01)
0054-0021-25	0054-0021	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate	TABLET, EXTENDED RELEASE	ORAL	20041028	N/A	ANDA	ANDA076832	Hikma Pharmaceuticals USA Inc.	LITHIUM CARBONATE	300 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0054-0021-25)
0054-0021-29	0054-0021	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate	TABLET, EXTENDED RELEASE	ORAL	20041028	N/A	ANDA	ANDA076832	Hikma Pharmaceuticals USA Inc.	LITHIUM CARBONATE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0054-0021-29)
68084-640-01	68084-640	HUMAN PRESCRIPTION DRUG	Lithium Carbonate	Lithium Carbonate	TABLET, EXTENDED RELEASE	ORAL	20141013	N/A	ANDA	ANDA076832	American Health Packaging	LITHIUM CARBONATE	300 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-640-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-640-11)