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=ANDA207566"
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
68094-690-30 68094-690 HUMAN PRESCRIPTION DRUG Azithromycin Dihydrate Azithromycin dihydrate TABLET, FILM COATED ORAL 20240215 N/A ANDA ANDA207566 Precision Dose, Inc. AZITHROMYCIN DIHYDRATE 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68094-690-30)
51224-222-30 51224-222 HUMAN PRESCRIPTION DRUG Azithromycin dihydrate Azithromycin dihydrate TABLET, FILM COATED ORAL 20190701 N/A ANDA ANDA207566 TAGI Pharma, Inc. AZITHROMYCIN DIHYDRATE 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (51224-222-30)
70518-3249-0 70518-3249 HUMAN PRESCRIPTION DRUG Azithromycin dihydrate Azithromycin dihydrate TABLET, FILM COATED ORAL 20211018 N/A ANDA ANDA207566 REMEDYREPACK INC. AZITHROMYCIN DIHYDRATE 600 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3249-0)
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