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
51079-923-20	51079-923	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	carbidopa and levodopa	TABLET, EXTENDED RELEASE	ORAL	19991201	N/A	ANDA	ANDA075091	Mylan Institutional Inc.	CARBIDOPA; LEVODOPA	50 mg/1; 200 mg/1	100 BLISTER PACK in 1 CARTON (51079-923-20) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (51079-923-01)
51079-978-20	51079-978	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	carbidopa and levodopa	TABLET, EXTENDED RELEASE	ORAL	20020201	N/A	ANDA	ANDA075091	Mylan Institutional Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	100 BLISTER PACK in 1 CARTON (51079-978-20) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (51079-978-01)
0378-0088-01	0378-0088	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	carbidopa and levodopa	TABLET, EXTENDED RELEASE	ORAL	20000426	N/A	ANDA	ANDA075091	Mylan Pharmaceuticals Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-0088-01)
0378-0094-01	0378-0094	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	carbidopa and levodopa	TABLET, EXTENDED RELEASE	ORAL	19991006	N/A	ANDA	ANDA075091	Mylan Pharmaceuticals Inc.	CARBIDOPA; LEVODOPA	50 mg/1; 200 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-0094-01)