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=NDA213871"
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
0069-0335-30 0069-0335 HUMAN PRESCRIPTION DRUG Cibinqo abrocitinib TABLET, FILM COATED ORAL 20220224 N/A NDA NDA213871 Pfizer Laboratories Div Pfizer Inc ABROCITINIB 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0069-0335-30)
0069-0435-30 0069-0435 HUMAN PRESCRIPTION DRUG Cibinqo abrocitinib TABLET, FILM COATED ORAL 20220224 N/A NDA NDA213871 Pfizer Laboratories Div Pfizer Inc ABROCITINIB 200 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0069-0435-30)
63539-236-14 63539-236 HUMAN PRESCRIPTION DRUG CIBINQO abrocitinib TABLET, FILM COATED ORAL 20220224 N/A NDA NDA213871 U.S. Pharmaceuticals ABROCITINIB 50 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (63539-236-14)
63539-336-14 63539-336 HUMAN PRESCRIPTION DRUG CIBINQO abrocitinib TABLET, FILM COATED ORAL 20220224 N/A NDA NDA213871 U.S. Pharmaceuticals ABROCITINIB 100 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (63539-336-14)
63539-436-14 63539-436 HUMAN PRESCRIPTION DRUG CIBINQO abrocitinib TABLET, FILM COATED ORAL 20220224 N/A NDA NDA213871 U.S. Pharmaceuticals ABROCITINIB 200 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (63539-436-14)
0069-0235-30 0069-0235 HUMAN PRESCRIPTION DRUG Cibinqo abrocitinib TABLET, FILM COATED ORAL 20220224 N/A NDA NDA213871 Pfizer Laboratories Div Pfizer Inc ABROCITINIB 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0069-0235-30)
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