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=ANDA210537"
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
62332-352-31 62332-352 HUMAN PRESCRIPTION DRUG Doxycycline Hyclate Doxycycline Hyclate TABLET, FILM COATED ORAL 20200305 N/A ANDA ANDA210537 Alembic Pharmaceuticals Inc. DOXYCYCLINE HYCLATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (62332-352-31)
62332-352-60 62332-352 HUMAN PRESCRIPTION DRUG Doxycycline Hyclate Doxycycline Hyclate TABLET, FILM COATED ORAL 20200305 N/A ANDA ANDA210537 Alembic Pharmaceuticals Inc. DOXYCYCLINE HYCLATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (62332-352-60)
62332-352-91 62332-352 HUMAN PRESCRIPTION DRUG Doxycycline Hyclate Doxycycline Hyclate TABLET, FILM COATED ORAL 20200305 N/A ANDA ANDA210537 Alembic Pharmaceuticals Inc. DOXYCYCLINE HYCLATE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (62332-352-91)
46708-352-31 46708-352 HUMAN PRESCRIPTION DRUG Doxycycline Hyclate Doxycycline Hyclate TABLET, FILM COATED ORAL 20200305 N/A ANDA ANDA210537 Alembic Pharmaceuticals Limited DOXYCYCLINE HYCLATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (46708-352-31)
46708-352-60 46708-352 HUMAN PRESCRIPTION DRUG Doxycycline Hyclate Doxycycline Hyclate TABLET, FILM COATED ORAL 20200305 N/A ANDA ANDA210537 Alembic Pharmaceuticals Limited DOXYCYCLINE HYCLATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (46708-352-60)
46708-352-91 46708-352 HUMAN PRESCRIPTION DRUG Doxycycline Hyclate Doxycycline Hyclate TABLET, FILM COATED ORAL 20200305 N/A ANDA ANDA210537 Alembic Pharmaceuticals Limited DOXYCYCLINE HYCLATE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (46708-352-91)
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