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
0093-1118-01	0093-1118	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20000817	N/A	ANDA	ANDA075665	Teva Pharmaceuticals USA, Inc.	ETODOLAC	600 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-1118-01)
0093-1122-01	0093-1122	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20010209	N/A	ANDA	ANDA075665	Teva Pharmaceuticals USA, Inc.	ETODOLAC	400 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-1122-01)
0093-7172-01	0093-7172	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20000811	N/A	ANDA	ANDA075665	Teva Pharmaceuticals USA, Inc.	ETODOLAC	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7172-01)
71205-140-30	71205-140	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181031	N/A	ANDA	ANDA075665	Proficient Rx LP	ETODOLAC	400 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-140-30)
71205-140-60	71205-140	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181031	N/A	ANDA	ANDA075665	Proficient Rx LP	ETODOLAC	400 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-140-60)
71205-140-90	71205-140	HUMAN PRESCRIPTION DRUG	Etodolac	Etodolac	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181031	N/A	ANDA	ANDA075665	Proficient Rx LP	ETODOLAC	400 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-140-90)