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
16571-157-01	16571-157	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	carbidopa and levodopa	TABLET, ORALLY DISINTEGRATING	ORAL	20250108	N/A	ANDA	ANDA078893	Rising Pharma Holdings, Inc.	CARBIDOPA; LEVODOPA	10 mg/1; 100 mg/1	100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (16571-157-01)
16571-158-01	16571-158	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	carbidopa and levodopa	TABLET, ORALLY DISINTEGRATING	ORAL	20250108	N/A	ANDA	ANDA078893	Rising Pharma Holdings, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (16571-158-01)
16571-159-01	16571-159	HUMAN PRESCRIPTION DRUG	Carbidopa and Levodopa	carbidopa and levodopa	TABLET, ORALLY DISINTEGRATING	ORAL	20250108	N/A	ANDA	ANDA078893	Rising Pharma Holdings, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 250 mg/1	100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (16571-159-01)