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
16571-692-01	16571-692	HUMAN PRESCRIPTION DRUG	CARBIDOPA, LEVODOPA AND ENTACAPONE	CARBIDOPA, LEVODOPA AND ENTACAPONE	TABLET, FILM COATED	ORAL	20210805	N/A	ANDA	ANDA213212	Rising Pharma Holdings, Inc.	CARBIDOPA; ENTACAPONE; LEVODOPA	31.25 mg/1; 200 mg/1; 125 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16571-692-01)
16571-693-01	16571-693	HUMAN PRESCRIPTION DRUG	CARBIDOPA, LEVODOPA AND ENTACAPONE	CARBIDOPA, LEVODOPA AND ENTACAPONE	TABLET, FILM COATED	ORAL	20210805	N/A	ANDA	ANDA213212	Rising Pharma Holdings, Inc.	CARBIDOPA; ENTACAPONE; LEVODOPA	37.5 mg/1; 200 mg/1; 150 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16571-693-01)
16571-694-01	16571-694	HUMAN PRESCRIPTION DRUG	CARBIDOPA, LEVODOPA AND ENTACAPONE	CARBIDOPA, LEVODOPA AND ENTACAPONE	TABLET, FILM COATED	ORAL	20210805	N/A	ANDA	ANDA213212	Rising Pharma Holdings, Inc.	CARBIDOPA; ENTACAPONE; LEVODOPA	50 mg/1; 200 mg/1; 200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16571-694-01)
16571-691-01	16571-691	HUMAN PRESCRIPTION DRUG	CARBIDOPA, LEVODOPA AND ENTACAPONE	CARBIDOPA, LEVODOPA AND ENTACAPONE	TABLET, FILM COATED	ORAL	20210805	N/A	ANDA	ANDA213212	Rising Pharma Holdings, Inc.	CARBIDOPA; ENTACAPONE; LEVODOPA	25 mg/1; 200 mg/1; 100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16571-691-01)
16571-690-01	16571-690	HUMAN PRESCRIPTION DRUG	CARBIDOPA, LEVODOPA AND ENTACAPONE	CARBIDOPA, LEVODOPA AND ENTACAPONE	TABLET, FILM COATED	ORAL	20210805	N/A	ANDA	ANDA213212	Rising Pharma Holdings, Inc.	CARBIDOPA; ENTACAPONE; LEVODOPA	18.75 mg/1; 200 mg/1; 75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16571-690-01)
16571-689-01	16571-689	HUMAN PRESCRIPTION DRUG	CARBIDOPA, LEVODOPA AND ENTACAPONE	CARBIDOPA, LEVODOPA AND ENTACAPONE	TABLET, FILM COATED	ORAL	20210805	N/A	ANDA	ANDA213212	Rising Pharma Holdings, Inc.	CARBIDOPA; ENTACAPONE; LEVODOPA	12.5 mg/1; 200 mg/1; 50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16571-689-01)