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=ANDA209044"
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
70518-3094-0 70518-3094 HUMAN PRESCRIPTION DRUG azithromycin AZITHROMYCIN MONOHYDRATE TABLET, FILM COATED ORAL 20210513 N/A ANDA ANDA209044 REMEDYREPACK INC. AZITHROMYCIN MONOHYDRATE 500 mg/1 2 POUCH in 1 BOX (70518-3094-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3094-1)
70518-3094-2 70518-3094 HUMAN PRESCRIPTION DRUG azithromycin AZITHROMYCIN MONOHYDRATE TABLET, FILM COATED ORAL 20240924 N/A ANDA ANDA209044 REMEDYREPACK INC. AZITHROMYCIN MONOHYDRATE 500 mg/1 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3094-2)
0527-2395-19 0527-2395 HUMAN PRESCRIPTION DRUG azithromycin AZITHROMYCIN MONOHYDRATE TABLET, FILM COATED ORAL 20190704 N/A ANDA ANDA209044 Lannett Company, Inc. AZITHROMYCIN MONOHYDRATE 500 mg/1 1 BLISTER PACK in 1 CARTON (0527-2395-19) / 3 TABLET, FILM COATED in 1 BLISTER PACK
0527-2395-32 0527-2395 HUMAN PRESCRIPTION DRUG azithromycin AZITHROMYCIN MONOHYDRATE TABLET, FILM COATED ORAL 20190704 N/A ANDA ANDA209044 Lannett Company, Inc. AZITHROMYCIN MONOHYDRATE 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0527-2395-32)
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