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=ANDA210129"
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
72189-657-30 72189-657 HUMAN PRESCRIPTION DRUG Amantadine HCL Amantadine HCL CAPSULE ORAL 20260115 N/A ANDA ANDA210129 Direct RX AMANTADINE HYDROCHLORIDE 100 mg/1 30 CAPSULE in 1 BOTTLE (72189-657-30)
10135-693-01 10135-693 HUMAN PRESCRIPTION DRUG Amantadine Hydrochloride Amantadine Hydrochloride CAPSULE, GELATIN COATED ORAL 20200301 N/A ANDA ANDA210129 Marlex Pharmaceuticals Inc AMANTADINE HYDROCHLORIDE 100 mg/1 100 CAPSULE, GELATIN COATED in 1 BOTTLE (10135-693-01)
10135-693-05 10135-693 HUMAN PRESCRIPTION DRUG Amantadine Hydrochloride Amantadine Hydrochloride CAPSULE, GELATIN COATED ORAL 20200301 N/A ANDA ANDA210129 Marlex Pharmaceuticals Inc AMANTADINE HYDROCHLORIDE 100 mg/1 500 CAPSULE, GELATIN COATED in 1 BOTTLE (10135-693-05)
16571-834-01 16571-834 HUMAN PRESCRIPTION DRUG Amantadine Hydrochloride Amantadine Hydrochloride CAPSULE ORAL 20220905 N/A ANDA ANDA210129 Rising Pharma Holdings, Inc. AMANTADINE HYDROCHLORIDE 100 mg/1 100 CAPSULE in 1 BOTTLE (16571-834-01)
16571-834-50 16571-834 HUMAN PRESCRIPTION DRUG Amantadine Hydrochloride Amantadine Hydrochloride CAPSULE ORAL 20220905 N/A ANDA ANDA210129 Rising Pharma Holdings, Inc. AMANTADINE HYDROCHLORIDE 100 mg/1 500 CAPSULE in 1 BOTTLE (16571-834-50)
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