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=ANDA210507"
符合检索条件的记录共 2 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
29300-313-22 29300-313 HUMAN OTC DRUG Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250101 N/A ANDA ANDA210507 Unichem Pharmaceuticals (USA), Inc. CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 5 mg/1; 120 mg/1 2 BLISTER PACK in 1 CARTON (29300-313-22) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (29300-313-61)
29300-313-24 29300-313 HUMAN OTC DRUG Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250101 N/A ANDA ANDA210507 Unichem Pharmaceuticals (USA), Inc. CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 5 mg/1; 120 mg/1 4 BLISTER PACK in 1 CARTON (29300-313-24) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (29300-313-61)
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