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
68071-2240-1	68071-2240	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET	ORAL	20200818	N/A	ANDA	ANDA078536	NuCare Pharmaceuticals,Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	100 TABLET in 1 BOTTLE (68071-2240-1)
63629-9154-1	63629-9154	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET	ORAL	20220127	N/A	ANDA	ANDA078536	Bryant Ranch Prepack	CARBIDOPA; LEVODOPA	25 mg/1; 250 mg/1	100 TABLET in 1 BOTTLE (63629-9154-1)
63629-2357-1	63629-2357	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET	ORAL	20081028	N/A	ANDA	ANDA078536	Bryant Ranch Prepack	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	100 TABLET in 1 BOTTLE (63629-2357-1)
62756-985-01	62756-985	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET	ORAL	20210812	N/A	ANDA	ANDA078536	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 250 mg/1	100 TABLET in 1 BOTTLE (62756-985-01)
62756-985-02	62756-985	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET	ORAL	20210812	N/A	ANDA	ANDA078536	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 250 mg/1	500 TABLET in 1 BOTTLE (62756-985-02)
62756-518-08	62756-518	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET	ORAL	20081028	N/A	ANDA	ANDA078536	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	100 TABLET in 1 BOTTLE (62756-518-08)
62756-518-13	62756-518	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET	ORAL	20081028	N/A	ANDA	ANDA078536	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	500 TABLET in 1 BOTTLE (62756-518-13)
62756-518-18	62756-518	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET	ORAL	20081028	N/A	ANDA	ANDA078536	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	1000 TABLET in 1 BOTTLE (62756-518-18)
62756-518-83	62756-518	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET	ORAL	20081028	N/A	ANDA	ANDA078536	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	30 TABLET in 1 BOTTLE (62756-518-83)
62756-518-88	62756-518	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET	ORAL	20081028	N/A	ANDA	ANDA078536	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	100 TABLET in 1 BOTTLE (62756-518-88)
63629-2356-1	63629-2356	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET	ORAL	20081028	N/A	ANDA	ANDA078536	Bryant Ranch Prepack	CARBIDOPA; LEVODOPA	25 mg/1; 100 mg/1	500 TABLET in 1 BOTTLE (63629-2356-1)
62756-517-88	62756-517	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET	ORAL	20081028	N/A	ANDA	ANDA078536	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	10 mg/1; 100 mg/1	100 TABLET in 1 BOTTLE (62756-517-88)
62756-517-08	62756-517	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET	ORAL	20081028	N/A	ANDA	ANDA078536	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	10 mg/1; 100 mg/1	100 TABLET in 1 BOTTLE (62756-517-08)
62756-517-13	62756-517	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET	ORAL	20081028	N/A	ANDA	ANDA078536	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	10 mg/1; 100 mg/1	500 TABLET in 1 BOTTLE (62756-517-13)
62756-517-18	62756-517	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET	ORAL	20081028	N/A	ANDA	ANDA078536	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	10 mg/1; 100 mg/1	1000 TABLET in 1 BOTTLE (62756-517-18)
62756-517-83	62756-517	HUMAN PRESCRIPTION DRUG	CARBIDOPA AND LEVODOPA	CARBIDOPA AND LEVODOPA	TABLET	ORAL	20081028	N/A	ANDA	ANDA078536	Sun Pharmaceutical Industries, Inc.	CARBIDOPA; LEVODOPA	10 mg/1; 100 mg/1	30 TABLET in 1 BOTTLE (62756-517-83)