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=ANDA079220"
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
71335-1879-9 71335-1879 HUMAN PRESCRIPTION DRUG ANASTROZOLE ANASTROZOLE TABLET ORAL 20211129 N/A ANDA ANDA079220 Bryant Ranch Prepack ANASTROZOLE 1 mg/1 14 TABLET in 1 BOTTLE (71335-1879-9)
51991-620-10 51991-620 HUMAN PRESCRIPTION DRUG ANASTROZOLE ANASTROZOLE TABLET ORAL 20100628 N/A ANDA ANDA079220 Breckenridge Pharmaceutical, Inc. ANASTROZOLE 1 mg/1 1000 TABLET in 1 BOTTLE (51991-620-10)
51991-620-33 51991-620 HUMAN PRESCRIPTION DRUG ANASTROZOLE ANASTROZOLE TABLET ORAL 20100628 N/A ANDA ANDA079220 Breckenridge Pharmaceutical, Inc. ANASTROZOLE 1 mg/1 30 TABLET in 1 BOTTLE (51991-620-33)
51991-620-90 51991-620 HUMAN PRESCRIPTION DRUG ANASTROZOLE ANASTROZOLE TABLET ORAL 20230401 N/A ANDA ANDA079220 Breckenridge Pharmaceutical, Inc. ANASTROZOLE 1 mg/1 90 TABLET in 1 BOTTLE (51991-620-90)
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