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=ANDA210609"
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
68788-8465-1 68788-8465 HUMAN PRESCRIPTION DRUG TADALAFIL tadalafil TABLET ORAL 20230623 N/A ANDA ANDA210609 Preferred Pharmaceuticals Inc. TADALAFIL 5 mg/1 15 TABLET in 1 BOTTLE (68788-8465-1)
68788-8465-2 68788-8465 HUMAN PRESCRIPTION DRUG TADALAFIL tadalafil TABLET ORAL 20230623 N/A ANDA ANDA210609 Preferred Pharmaceuticals Inc. TADALAFIL 5 mg/1 20 TABLET in 1 BOTTLE (68788-8465-2)
68788-8664-1 68788-8664 HUMAN PRESCRIPTION DRUG TADALAFIL tadalafil TABLET ORAL 20240513 N/A ANDA ANDA210609 Preferred Pharmaceuticals Inc. TADALAFIL 20 mg/1 15 TABLET in 1 BOTTLE (68788-8664-1)
68788-8664-3 68788-8664 HUMAN PRESCRIPTION DRUG TADALAFIL tadalafil TABLET ORAL 20240513 N/A ANDA ANDA210609 Preferred Pharmaceuticals Inc. TADALAFIL 20 mg/1 30 TABLET in 1 BOTTLE (68788-8664-3)
68788-8664-7 68788-8664 HUMAN PRESCRIPTION DRUG TADALAFIL tadalafil TABLET ORAL 20240513 N/A ANDA ANDA210609 Preferred Pharmaceuticals Inc. TADALAFIL 20 mg/1 7 TABLET in 1 BOTTLE (68788-8664-7)
70518-3864-0 70518-3864 HUMAN PRESCRIPTION DRUG TADALAFIL tadalafil TABLET ORAL 20230918 N/A ANDA ANDA210609 REMEDYREPACK INC. TADALAFIL 5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (70518-3864-0)
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