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=ANDA210859"
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
31722-628-01 31722-628 HUMAN PRESCRIPTION DRUG EZETIMIBE EZETIMIBE TABLET ORAL 20220213 N/A ANDA ANDA210859 Camber Pharmaceuticals, Inc. EZETIMIBE 10 mg/1 100 TABLET in 1 BOTTLE (31722-628-01)
31722-628-30 31722-628 HUMAN PRESCRIPTION DRUG EZETIMIBE EZETIMIBE TABLET ORAL 20220213 N/A ANDA ANDA210859 Camber Pharmaceuticals, Inc. EZETIMIBE 10 mg/1 30 TABLET in 1 BOTTLE (31722-628-30)
31722-628-31 31722-628 HUMAN PRESCRIPTION DRUG EZETIMIBE EZETIMIBE TABLET ORAL 20220213 N/A ANDA ANDA210859 Camber Pharmaceuticals, Inc. EZETIMIBE 10 mg/1 100 BLISTER PACK in 1 CARTON (31722-628-31) / 10 TABLET in 1 BLISTER PACK
31722-628-32 31722-628 HUMAN PRESCRIPTION DRUG EZETIMIBE EZETIMIBE TABLET ORAL 20220213 N/A ANDA ANDA210859 Camber Pharmaceuticals, Inc. EZETIMIBE 10 mg/1 70 BLISTER PACK in 1 CARTON (31722-628-32) / 7 TABLET in 1 BLISTER PACK
31722-628-90 31722-628 HUMAN PRESCRIPTION DRUG EZETIMIBE EZETIMIBE TABLET ORAL 20220213 N/A ANDA ANDA210859 Camber Pharmaceuticals, Inc. EZETIMIBE 10 mg/1 90 TABLET in 1 BOTTLE (31722-628-90)
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