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)
检索条件:" 注册申请号=ANDA218535"
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
46708-795-91 46708-795 HUMAN PRESCRIPTION DRUG carbidopa, levodopa and entacapone carbidopa, levodopa and entacapone TABLET, FILM COATED ORAL 20260212 N/A ANDA ANDA218535 Alembic Pharmaceuticals Limited CARBIDOPA; ENTACAPONE; LEVODOPA 12.5 mg/1; 200 mg/1; 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (46708-795-91)
46708-799-31 46708-799 HUMAN PRESCRIPTION DRUG carbidopa, levodopa and entacapone carbidopa, levodopa and entacapone TABLET, FILM COATED ORAL 20260212 N/A ANDA ANDA218535 Alembic Pharmaceuticals Limited CARBIDOPA; ENTACAPONE; LEVODOPA 37.5 mg/1; 200 mg/1; 150 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (46708-799-31)
46708-799-91 46708-799 HUMAN PRESCRIPTION DRUG carbidopa, levodopa and entacapone carbidopa, levodopa and entacapone TABLET, FILM COATED ORAL 20260212 N/A ANDA ANDA218535 Alembic Pharmaceuticals Limited CARBIDOPA; ENTACAPONE; LEVODOPA 37.5 mg/1; 200 mg/1; 150 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (46708-799-91)
46708-800-91 46708-800 HUMAN PRESCRIPTION DRUG carbidopa, levodopa and entacapone carbidopa, levodopa and entacapone TABLET, FILM COATED ORAL 20260212 N/A ANDA ANDA218535 Alembic Pharmaceuticals Limited CARBIDOPA; ENTACAPONE; LEVODOPA 50 mg/1; 200 mg/1; 200 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (46708-800-91)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase