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=ANDA078969"
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
51991-735-20 51991-735 HUMAN PRESCRIPTION DRUG Granisetron Hydrochloride Granisetron Hydrochloride TABLET ORAL 20090622 N/A ANDA ANDA078969 Breckenridge Pharmaceutical, Inc. GRANISETRON HYDROCHLORIDE 1 mg/1 2 BLISTER PACK in 1 CARTON (51991-735-20) / 10 TABLET in 1 BLISTER PACK
51991-735-32 51991-735 HUMAN PRESCRIPTION DRUG Granisetron Hydrochloride Granisetron Hydrochloride TABLET ORAL 20090622 N/A ANDA ANDA078969 Breckenridge Pharmaceutical, Inc. GRANISETRON HYDROCHLORIDE 1 mg/1 1 BLISTER PACK in 1 CARTON (51991-735-32) / 2 TABLET in 1 BLISTER PACK
63850-0005-1 63850-0005 HUMAN PRESCRIPTION DRUG Granisetron hydrochloride Granisetron hydrochloride TABLET, FILM COATED ORAL 20090622 N/A ANDA ANDA078969 Natco Pharma Limited GRANISETRON HYDROCHLORIDE 1 mg/1 10 TABLET, FILM COATED in 1 BLISTER PACK (63850-0005-1)
63850-0005-2 63850-0005 HUMAN PRESCRIPTION DRUG Granisetron hydrochloride Granisetron hydrochloride TABLET, FILM COATED ORAL 20090622 N/A ANDA ANDA078969 Natco Pharma Limited GRANISETRON HYDROCHLORIDE 1 mg/1 2 TABLET, FILM COATED in 1 BLISTER PACK (63850-0005-2)
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