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=ANDA210719"
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
69842-415-62 69842-415 HUMAN OTC DRUG allergy relief d cetirizine hydrochloride, pseudoephedrine hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200401 N/A ANDA ANDA210719 CVS Pharmacy CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 5 mg/1; 120 mg/1 24 BLISTER PACK in 1 CARTON (69842-415-62) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
0363-4923-53 0363-4923 HUMAN OTC DRUG allergy relief D12 Cetirizine hydrochloride, Pseudoephedrine hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20211020 N/A ANDA ANDA210719 Walgreen Company CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 5 mg/1; 120 mg/1 12 BLISTER PACK in 1 CARTON (0363-4923-53) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
0363-4923-62 0363-4923 HUMAN OTC DRUG allergy relief D12 Cetirizine hydrochloride, Pseudoephedrine hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20211020 N/A ANDA ANDA210719 Walgreen Company CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 5 mg/1; 120 mg/1 24 BLISTER PACK in 1 CARTON (0363-4923-62) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
11822-3009-0 11822-3009 HUMAN OTC DRUG allergy relief-D Cetirizine hydrochloride, Pseudoephedrine hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20230501 N/A ANDA ANDA210719 Rite Aid Corporation CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 5 mg/1; 120 mg/1 24 BLISTER PACK in 1 CARTON (11822-3009-0) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase