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
42291-488-10	42291-488	HUMAN PRESCRIPTION DRUG	Carbidopa and levodopa	Carbidopa and levodopa	TABLET	ORAL	20240221	N/A	ANDA	ANDA074260	AvKARE	CARBIDOPA; LEVODOPA	25 mg/1; 250 mg/1	1000 TABLET in 1 BOTTLE (42291-488-10)
0093-9703-01	0093-9703	HUMAN PRESCRIPTION DRUG	Carbidopa and levodopa	Carbidopa and levodopa	TABLET	ORAL	20240305	N/A	ANDA	ANDA074260	Teva Pharmaceuticals USA, Inc.	CARBIDOPA HYDRATE; LEVODOPA	25 mg/1; 250 mg/1	100 TABLET in 1 BOTTLE (0093-9703-01)
0093-9703-05	0093-9703	HUMAN PRESCRIPTION DRUG	Carbidopa and levodopa	Carbidopa and levodopa	TABLET	ORAL	20231215	N/A	ANDA	ANDA074260	Teva Pharmaceuticals USA, Inc.	CARBIDOPA HYDRATE; LEVODOPA	25 mg/1; 250 mg/1	500 TABLET in 1 BOTTLE (0093-9703-05)
0093-9703-10	0093-9703	HUMAN PRESCRIPTION DRUG	Carbidopa and levodopa	Carbidopa and levodopa	TABLET	ORAL	20240208	N/A	ANDA	ANDA074260	Teva Pharmaceuticals USA, Inc.	CARBIDOPA HYDRATE; LEVODOPA	25 mg/1; 250 mg/1	1000 TABLET in 1 BOTTLE (0093-9703-10)