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
68084-282-01	68084-282	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	Carbidopa and Levodopa	TABLET, EXTENDED RELEASE	ORAL	20080901	N/A	ANDA	ANDA077828	American Health Packaging	CARBIDOPA; LEVODOPA	50 mg/1; 200 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-282-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-282-11)
68084-281-01	68084-281	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	Carbidopa and Levodopa	TABLET, EXTENDED RELEASE	ORAL	20080901	N/A	ANDA	ANDA077828	American Health Packaging	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-281-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-281-11)
62756-461-08	62756-461	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, EXTENDED RELEASE	ORAL	20070823	N/A	ANDA	ANDA077828	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-461-08)
62756-461-18	62756-461	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, EXTENDED RELEASE	ORAL	20070823	N/A	ANDA	ANDA077828	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-461-18)
62756-461-83	62756-461	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, EXTENDED RELEASE	ORAL	20070823	N/A	ANDA	ANDA077828	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-461-83)
62756-461-88	62756-461	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, EXTENDED RELEASE	ORAL	20070823	N/A	ANDA	ANDA077828	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-461-88)
62756-457-08	62756-457	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, EXTENDED RELEASE	ORAL	20070823	N/A	ANDA	ANDA077828	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	50 mg/1; 200 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-457-08)
62756-457-18	62756-457	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, EXTENDED RELEASE	ORAL	20070823	N/A	ANDA	ANDA077828	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	50 mg/1; 200 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-457-18)
62756-457-83	62756-457	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, EXTENDED RELEASE	ORAL	20070823	N/A	ANDA	ANDA077828	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	50 mg/1; 200 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-457-83)
62756-457-88	62756-457	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET, EXTENDED RELEASE	ORAL	20070823	N/A	ANDA	ANDA077828	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	50 mg/1; 200 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-457-88)