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
68071-3853-8 68071-3853 HUMAN PRESCRIPTION DRUG ANASTROZOLE ANASTROZOLE TABLET ORAL 20250527 N/A ANDA ANDA079220 NuCare Pharmaceuticals, Inc. ANASTROZOLE 1 mg/1 8 TABLET in 1 BOTTLE (68071-3853-8)
63850-0010-1 63850-0010 HUMAN PRESCRIPTION DRUG Anastrozole Anastrozole TABLET ORAL 20100628 N/A ANDA ANDA079220 Natco Pharma Limited ANASTROZOLE 1 mg/1 30 TABLET in 1 BOTTLE (63850-0010-1)
63850-0010-2 63850-0010 HUMAN PRESCRIPTION DRUG Anastrozole Anastrozole TABLET ORAL 20100628 N/A ANDA ANDA079220 Natco Pharma Limited ANASTROZOLE 1 mg/1 1000 TABLET in 1 BOTTLE (63850-0010-2)
43063-383-15 43063-383 HUMAN PRESCRIPTION DRUG ANASTROZOLE ANASTROZOLE TABLET ORAL 20180820 N/A ANDA ANDA079220 PD-Rx Pharmaceuticals, Inc. ANASTROZOLE 1 mg/1 15 TABLET in 1 BOTTLE, PLASTIC (43063-383-15)
43063-383-06 43063-383 HUMAN PRESCRIPTION DRUG ANASTROZOLE ANASTROZOLE TABLET ORAL 20180823 N/A ANDA ANDA079220 PD-Rx Pharmaceuticals, Inc. ANASTROZOLE 1 mg/1 6 TABLET in 1 BOTTLE, PLASTIC (43063-383-06)
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