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=ANDA212601"
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
62332-478-31 62332-478 HUMAN PRESCRIPTION DRUG ENTACAPONE ENTACAPONE TABLET, FILM COATED ORAL 20220106 N/A ANDA ANDA212601 Alembic Pharmaceuticals Inc. ENTACAPONE 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (62332-478-31)
62332-478-91 62332-478 HUMAN PRESCRIPTION DRUG ENTACAPONE ENTACAPONE TABLET, FILM COATED ORAL 20220106 N/A ANDA ANDA212601 Alembic Pharmaceuticals Inc. ENTACAPONE 200 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (62332-478-91)
46708-478-91 46708-478 HUMAN PRESCRIPTION DRUG ENTACAPONE ENTACAPONE TABLET, FILM COATED ORAL 20220106 N/A ANDA ANDA212601 Alembic Pharmaceuticals Limited ENTACAPONE 200 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (46708-478-91)
46708-478-31 46708-478 HUMAN PRESCRIPTION DRUG ENTACAPONE ENTACAPONE TABLET, FILM COATED ORAL 20220106 N/A ANDA ANDA212601 Alembic Pharmaceuticals Limited ENTACAPONE 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (46708-478-31)
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