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
0615-8555-39	0615-8555	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	Carbidopa and Levodopa	TABLET	ORAL	20241024	N/A	ANDA	ANDA073618	NCS HealthCare of KY, LLC dba Vangard Labs	CARBIDOPA; LEVODOPA	10 mg/1; 100 mg/1	30 TABLET in 1 BLISTER PACK (0615-8555-39)
51862-855-01	51862-855	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	Carbidopa and Levodopa	TABLET	ORAL	20180716	N/A	ANDA	ANDA073618	Mayne Pharma Commercial LLC	CARBIDOPA; LEVODOPA	10 mg/1; 100 mg/1	100 TABLET in 1 BOTTLE (51862-855-01)
51862-855-05	51862-855	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	Carbidopa and Levodopa	TABLET	ORAL	20180716	N/A	ANDA	ANDA073618	Mayne Pharma Commercial LLC	CARBIDOPA; LEVODOPA	10 mg/1; 100 mg/1	500 TABLET in 1 BOTTLE (51862-855-05)
75907-022-01	75907-022	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	Carbidopa and Levodopa	TABLET	ORAL	20240501	N/A	ANDA	ANDA073618	Dr. Reddy's Laboratories Inc	CARBIDOPA; LEVODOPA	10 mg/1; 100 mg/1	100 TABLET in 1 BOTTLE (75907-022-01)