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=NDA017854"
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
62559-165-01 62559-165 HUMAN PRESCRIPTION DRUG Reglan Metoclopramide Hydrochloride TABLET ORAL 20110705 N/A NDA NDA017854 ANI Pharmaceuticals, Inc. METOCLOPRAMIDE HYDROCHLORIDE 5 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (62559-165-01)
62559-166-01 62559-166 HUMAN PRESCRIPTION DRUG Reglan Metoclopramide Hydrochloride TABLET ORAL 20110705 N/A NDA NDA017854 ANI Pharmaceuticals, Inc. METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (62559-166-01)
62559-295-01 62559-295 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 20211213 N/A NDA AUTHORIZED GENERIC NDA017854 ANI Pharmaceuticals, Inc. METOCLOPRAMIDE HYDROCHLORIDE 5 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (62559-295-01)
62559-296-01 62559-296 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 20211213 N/A NDA AUTHORIZED GENERIC NDA017854 ANI Pharmaceuticals, Inc. METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (62559-296-01)
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