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=ANDA078933"
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
0363-1794-38 0363-1794 HUMAN OTC DRUG Allergy Relief Cetirizine Hydrochloride TABLET ORAL 20231025 N/A ANDA ANDA078933 WALGREENS CETIRIZINE HYDROCHLORIDE 10 mg/1 1 BLISTER PACK in 1 CARTON (0363-1794-38) / 5 TABLET in 1 BLISTER PACK
0363-1794-46 0363-1794 HUMAN OTC DRUG Allergy Relief Cetirizine Hydrochloride TABLET ORAL 20231025 N/A ANDA ANDA078933 WALGREENS CETIRIZINE HYDROCHLORIDE 10 mg/1 1 BLISTER PACK in 1 CARTON (0363-1794-46) / 14 TABLET in 1 BLISTER PACK
49483-682-01 49483-682 HUMAN OTC DRUG Cetirizine Hydrochloride Cetirizine Hydrochloride TABLET ORAL 20220530 N/A ANDA ANDA078933 TIME CAP LABORATORIES, INC. CETIRIZINE HYDROCHLORIDE 5 mg/1 100 TABLET in 1 BOTTLE (49483-682-01)
49483-692-01 49483-692 HUMAN OTC DRUG Cetirizine Hydrochloride Tablets,10 mg Cetirizine Hydrochloride TABLET ORAL 20240311 N/A ANDA ANDA078933 TIME CAP LABORATORIES, INC. CETIRIZINE HYDROCHLORIDE 10 mg/1 100 TABLET in 1 BOTTLE (49483-692-01)
49483-692-20 49483-692 HUMAN OTC DRUG Cetirizine Hydrochloride Tablets,10 mg Cetirizine Hydrochloride TABLET ORAL 20240311 N/A ANDA ANDA078933 TIME CAP LABORATORIES, INC. CETIRIZINE HYDROCHLORIDE 10 mg/1 200 TABLET in 1 BOTTLE (49483-692-20)
49483-692-50 49483-692 HUMAN OTC DRUG Cetirizine Hydrochloride Tablets,10 mg Cetirizine Hydrochloride TABLET ORAL 20220530 N/A ANDA ANDA078933 TIME CAP LABORATORIES, INC. CETIRIZINE HYDROCHLORIDE 10 mg/1 500 TABLET in 1 BOTTLE (49483-692-50)
49483-692-65 49483-692 HUMAN OTC DRUG Cetirizine Hydrochloride Tablets,10 mg Cetirizine Hydrochloride TABLET ORAL 20220212 N/A ANDA ANDA078933 TIME CAP LABORATORIES, INC. CETIRIZINE HYDROCHLORIDE 10 mg/1 365 TABLET in 1 BOTTLE (49483-692-65)
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