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=ANDA077442"
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
21130-204-69 21130-204 HUMAN OTC DRUG Pseudoephedrine Hydrochloride Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20060428 N/A ANDA ANDA077442 Safeway Inc. PSEUDOEPHEDRINE HYDROCHLORIDE 120 mg/1 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (21130-204-69)
0363-0204-20 0363-0204 HUMAN OTC DRUG Pseudoephedrine Hydrochloride Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190116 N/A ANDA ANDA077442 Walgreen Company PSEUDOEPHEDRINE HYDROCHLORIDE 120 mg/1 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0363-0204-20)
0363-0204-69 0363-0204 HUMAN OTC DRUG Pseudoephedrine Hydrochloride Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20060428 N/A ANDA ANDA077442 Walgreen Company PSEUDOEPHEDRINE HYDROCHLORIDE 120 mg/1 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0363-0204-69)
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