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=ANDA210215"
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
10135-692-01 10135-692 HUMAN PRESCRIPTION DRUG Amantadine Hydrochloride Amantadine Hydrochloride TABLET ORAL 20200301 N/A ANDA ANDA210215 Marlex Pharmaceuticals Inc AMANTADINE HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (10135-692-01)
10135-692-05 10135-692 HUMAN PRESCRIPTION DRUG Amantadine Hydrochloride Amantadine Hydrochloride TABLET ORAL 20200301 N/A ANDA ANDA210215 Marlex Pharmaceuticals Inc AMANTADINE HYDROCHLORIDE 100 mg/1 500 TABLET in 1 BOTTLE (10135-692-05)
24689-112-01 24689-112 HUMAN PRESCRIPTION DRUG AMANTADINE HYDROCHLORIDE amantadine hydrochloride TABLET ORAL 20240601 N/A ANDA ANDA210215 Apnar Pharma LP AMANTADINE HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (24689-112-01)
24689-112-02 24689-112 HUMAN PRESCRIPTION DRUG AMANTADINE HYDROCHLORIDE amantadine hydrochloride TABLET ORAL 20240601 N/A ANDA ANDA210215 Apnar Pharma LP AMANTADINE HYDROCHLORIDE 100 mg/1 500 TABLET in 1 BOTTLE (24689-112-02)
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