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
62135-910-60	62135-910	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20240829	N/A	ANDA	ANDA209888	Chartwell RX, LLC	ETODOLAC	400 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (62135-910-60)
62135-911-60	62135-911	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20240829	N/A	ANDA	ANDA209888	Chartwell RX, LLC	ETODOLAC	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (62135-911-60)
42799-112-01	42799-112	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20181207	N/A	ANDA	ANDA209888	Edenbridge Pharmaceuticals LLC.	ETODOLAC	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (42799-112-01)
42799-111-01	42799-111	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20181207	N/A	ANDA	ANDA209888	Edenbridge Pharmaceuticals LLC.	ETODOLAC	400 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (42799-111-01)