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
76385-119-01	76385-119	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20210801	N/A	ANDA	ANDA210704	Bayshore Pharmaceuticals, LLC	ETODOLAC	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76385-119-01)
50090-6739-5	50090-6739	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20231012	N/A	ANDA	ANDA210704	A-S Medication Solutions	ETODOLAC	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-6739-5)
76385-118-01	76385-118	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20210801	N/A	ANDA	ANDA210704	Bayshore Pharmaceuticals, LLC	ETODOLAC	400 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76385-118-01)
68788-8580-6	68788-8580	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20240205	N/A	ANDA	ANDA210704	Preferred Pharmaceuticals Inc.	ETODOLAC	400 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68788-8580-6)
83008-073-60	83008-073	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20240725	N/A	ANDA	ANDA210704	Quality Care Products, LLC	ETODOLAC	400 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (83008-073-60)
71610-850-53	71610-850	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20240821	N/A	ANDA	ANDA210704	Aphena Pharma Solutions - Tennessee, LLC	ETODOLAC	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71610-850-53)
71335-2259-1	71335-2259	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20231030	N/A	ANDA	ANDA210704	Bryant Ranch Prepack	ETODOLAC	400 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-2259-1)
71335-2259-2	71335-2259	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20231030	N/A	ANDA	ANDA210704	Bryant Ranch Prepack	ETODOLAC	400 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-2259-2)
71335-2259-3	71335-2259	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20231030	N/A	ANDA	ANDA210704	Bryant Ranch Prepack	ETODOLAC	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2259-3)
71335-2259-4	71335-2259	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20231030	N/A	ANDA	ANDA210704	Bryant Ranch Prepack	ETODOLAC	400 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2259-4)
71335-2259-5	71335-2259	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20231030	N/A	ANDA	ANDA210704	Bryant Ranch Prepack	ETODOLAC	400 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2259-5)
71335-2259-6	71335-2259	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20231030	N/A	ANDA	ANDA210704	Bryant Ranch Prepack	ETODOLAC	400 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2259-6)
71335-2259-7	71335-2259	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20231030	N/A	ANDA	ANDA210704	Bryant Ranch Prepack	ETODOLAC	400 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (71335-2259-7)
71335-2259-8	71335-2259	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED	ORAL	20231030	N/A	ANDA	ANDA210704	Bryant Ranch Prepack	ETODOLAC	400 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-2259-8)