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=ANDA208202"
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
62332-233-30 62332-233 HUMAN PRESCRIPTION DRUG VILAZODONE HYDROCHLORIDE VILAZODONE HYDROCHLORIDE TABLET, FILM COATED ORAL 20220604 N/A ANDA ANDA208202 Alembic Pharmaceuticals Inc. VILAZODONE HYDROCHLORIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (62332-233-30)
62332-233-71 62332-233 HUMAN PRESCRIPTION DRUG VILAZODONE HYDROCHLORIDE VILAZODONE HYDROCHLORIDE TABLET, FILM COATED ORAL 20220604 N/A ANDA ANDA208202 Alembic Pharmaceuticals Inc. VILAZODONE HYDROCHLORIDE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (62332-233-71)
62332-233-90 62332-233 HUMAN PRESCRIPTION DRUG VILAZODONE HYDROCHLORIDE VILAZODONE HYDROCHLORIDE TABLET, FILM COATED ORAL 20220604 N/A ANDA ANDA208202 Alembic Pharmaceuticals Inc. VILAZODONE HYDROCHLORIDE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (62332-233-90)
62332-233-91 62332-233 HUMAN PRESCRIPTION DRUG VILAZODONE HYDROCHLORIDE VILAZODONE HYDROCHLORIDE TABLET, FILM COATED ORAL 20220604 N/A ANDA ANDA208202 Alembic Pharmaceuticals Inc. VILAZODONE HYDROCHLORIDE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (62332-233-91)
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