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
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)
0093-9702-01	0093-9702	HUMAN PRESCRIPTION DRUG	Carbidopa and levodopa	Carbidopa and levodopa	TABLET	ORAL	20220225	N/A	ANDA	ANDA074260	Teva Pharmaceuticals USA, Inc.	CARBIDOPA HYDRATE; LEVODOPA	25 mg/1; 100 mg/1	100 TABLET in 1 BOTTLE (0093-9702-01)
0093-9702-05	0093-9702	HUMAN PRESCRIPTION DRUG	Carbidopa and levodopa	Carbidopa and levodopa	TABLET	ORAL	20220324	N/A	ANDA	ANDA074260	Teva Pharmaceuticals USA, Inc.	CARBIDOPA HYDRATE; LEVODOPA	25 mg/1; 100 mg/1	500 TABLET in 1 BOTTLE (0093-9702-05)
0093-9701-01	0093-9701	HUMAN PRESCRIPTION DRUG	Carbidopa and levodopa	Carbidopa and levodopa	TABLET	ORAL	20220118	N/A	ANDA	ANDA074260	Teva Pharmaceuticals USA, Inc.	CARBIDOPA HYDRATE; LEVODOPA	10 mg/1; 100 mg/1	100 TABLET in 1 BOTTLE (0093-9701-01)