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=ANDA090958"
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
69097-209-02 69097-209 HUMAN PRESCRIPTION DRUG EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE TABLET, FILM COATED ORAL 20210330 N/A ANDA ANDA090958 Cipla USA Inc. EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE 200 mg/1; 300 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69097-209-02)
69097-741-02 69097-741 HUMAN PRESCRIPTION DRUG EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE TABLET, FILM COATED ORAL 20211101 N/A ANDA ANDA090958 Cipla USA Inc. EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE 200 mg/1; 300 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69097-741-02)
76282-677-30 76282-677 HUMAN PRESCRIPTION DRUG EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE TABLET, FILM COATED ORAL 20210406 N/A ANDA ANDA090958 Exelan Pharmaceuticals, Inc. EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE 200 mg/1; 300 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76282-677-30)
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