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
75907-021-01	75907-021	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	Carbidopa and Levodopa	TABLET	ORAL	20240501	N/A	ANDA	ANDA073607	Dr. Reddy's Laboratories Inc	CARBIDOPA; LEVODOPA	25 mg/1; 250 mg/1	100 TABLET in 1 BOTTLE (75907-021-01)
51862-858-01	51862-858	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	Carbidopa and Levodopa	TABLET	ORAL	20180716	N/A	ANDA	ANDA073607	Mayne Pharma Commercial LLC	CARBIDOPA; LEVODOPA	25 mg/1; 250 mg/1	100 TABLET in 1 BOTTLE (51862-858-01)
51862-858-05	51862-858	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	Carbidopa and Levodopa	TABLET	ORAL	20180716	N/A	ANDA	ANDA073607	Mayne Pharma Commercial LLC	CARBIDOPA; LEVODOPA	25 mg/1; 250 mg/1	500 TABLET in 1 BOTTLE (51862-858-05)
51862-858-10	51862-858	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	Carbidopa and Levodopa	TABLET	ORAL	20180716	N/A	ANDA	ANDA073607	Mayne Pharma Commercial LLC	CARBIDOPA; LEVODOPA	25 mg/1; 250 mg/1	1000 TABLET in 1 BOTTLE (51862-858-10)
0615-8275-39	0615-8275	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	Carbidopa and Levodopa	TABLET	ORAL	20190305	N/A	ANDA	ANDA073607	NCS HealthCare of KY, LLC dba Vangard Labs	CARBIDOPA; LEVODOPA	25 mg/1; 250 mg/1	30 TABLET in 1 BLISTER PACK (0615-8275-39)