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=ANDA210375"
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
11673-847-35 11673-847 HUMAN OTC DRUG levocetirizine dihydrochloride levocetirizine dihydrochloride TABLET, COATED ORAL 20181231 N/A ANDA ANDA210375 Target Corporation LEVOCETIRIZINE DIHYDROCHLORIDE 5 mg/1 1 BOTTLE in 1 CARTON (11673-847-35) / 35 TABLET, COATED in 1 BOTTLE
68391-955-11 68391-955 HUMAN OTC DRUG levocetirizine dihydrochloride levocetirizine dihydrochloride TABLET, COATED ORAL 20240815 N/A ANDA ANDA210375 BJWC (Berkley & Jensen / BJ'S) LEVOCETIRIZINE DIHYDROCHLORIDE 5 mg/1 2 BOTTLE in 1 PACKAGE (68391-955-11) / 55 TABLET, COATED in 1 BOTTLE (68391-955-55)
21130-732-10 21130-732 HUMAN OTC DRUG Allergy Relief levocetirizine dihydrochloride TABLET, COATED ORAL 20180630 N/A ANDA ANDA210375 Albertsons Companies LEVOCETIRIZINE DIHYDROCHLORIDE 5 mg/1 2 BLISTER PACK in 1 CARTON (21130-732-10) / 5 TABLET, COATED in 1 BLISTER PACK
21130-732-35 21130-732 HUMAN OTC DRUG Allergy Relief levocetirizine dihydrochloride TABLET, COATED ORAL 20180630 N/A ANDA ANDA210375 Albertsons Companies LEVOCETIRIZINE DIHYDROCHLORIDE 5 mg/1 1 BOTTLE in 1 CARTON (21130-732-35) / 35 TABLET, COATED in 1 BOTTLE
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