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
71335-0399-6	71335-0399	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20240905	N/A	ANDA	ANDA076004	Bryant Ranch Prepack	ETODOLAC	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-0399-6)
71335-0399-7	71335-0399	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20240905	N/A	ANDA	ANDA076004	Bryant Ranch Prepack	ETODOLAC	500 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-0399-7)
63629-8805-1	63629-8805	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20030501	N/A	ANDA	ANDA076004	Bryant Ranch Prepack	ETODOLAC	400 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (63629-8805-1)
71335-0399-1	71335-0399	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20240905	N/A	ANDA	ANDA076004	Bryant Ranch Prepack	ETODOLAC	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0399-1)
71335-0399-2	71335-0399	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20240905	N/A	ANDA	ANDA076004	Bryant Ranch Prepack	ETODOLAC	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0399-2)
80425-0190-2	80425-0190	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20240217	N/A	ANDA	ANDA076004	Advanced Rx Pharmacy of Tennessee, LLC	ETODOLAC	400 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0190-2)