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
47335-188-08	47335-188	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, ORALLY DISINTEGRATING	ORAL	20141215	N/A	ANDA	ANDA078690	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 250 mg/1	100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-188-08)
47335-188-18	47335-188	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, ORALLY DISINTEGRATING	ORAL	20141215	N/A	ANDA	ANDA078690	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 250 mg/1	1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-188-18)
47335-188-83	47335-188	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, ORALLY DISINTEGRATING	ORAL	20141215	N/A	ANDA	ANDA078690	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 250 mg/1	30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-188-83)
47335-188-88	47335-188	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, ORALLY DISINTEGRATING	ORAL	20141215	N/A	ANDA	ANDA078690	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 250 mg/1	100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-188-88)
47335-187-08	47335-187	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, ORALLY DISINTEGRATING	ORAL	20141215	N/A	ANDA	ANDA078690	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-187-08)
47335-187-18	47335-187	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, ORALLY DISINTEGRATING	ORAL	20141215	N/A	ANDA	ANDA078690	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-187-18)
47335-187-83	47335-187	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, ORALLY DISINTEGRATING	ORAL	20141215	N/A	ANDA	ANDA078690	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-187-83)
47335-187-88	47335-187	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, ORALLY DISINTEGRATING	ORAL	20141215	N/A	ANDA	ANDA078690	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-187-88)
47335-186-08	47335-186	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, ORALLY DISINTEGRATING	ORAL	20141215	N/A	ANDA	ANDA078690	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	10 mg/1; 100 mg/1	100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-186-08)
47335-186-18	47335-186	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, ORALLY DISINTEGRATING	ORAL	20141215	N/A	ANDA	ANDA078690	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	10 mg/1; 100 mg/1	1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-186-18)
47335-186-83	47335-186	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, ORALLY DISINTEGRATING	ORAL	20141215	N/A	ANDA	ANDA078690	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	10 mg/1; 100 mg/1	30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-186-83)
47335-186-88	47335-186	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, ORALLY DISINTEGRATING	ORAL	20141215	N/A	ANDA	ANDA078690	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	10 mg/1; 100 mg/1	100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-186-88)