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=ANDA211556"
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
72789-238-01 72789-238 HUMAN PRESCRIPTION DRUG Acetazolamide Acetazolamide TABLET ORAL 20220310 N/A ANDA ANDA211556 PD-Rx Pharmaceuticals, Inc. ACETAZOLAMIDE 125 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (72789-238-01)
71930-008-12 71930-008 HUMAN PRESCRIPTION DRUG Acetazolamide Acetazolamide TABLET ORAL 20200130 N/A ANDA ANDA211556 Eywa Pharma Inc ACETAZOLAMIDE 125 mg/1 100 TABLET in 1 BOTTLE (71930-008-12)
71930-009-12 71930-009 HUMAN PRESCRIPTION DRUG Acetazolamide Acetazolamide TABLET ORAL 20200130 N/A ANDA ANDA211556 Eywa Pharma Inc ACETAZOLAMIDE 250 mg/1 100 TABLET in 1 BOTTLE (71930-009-12)
72789-237-01 72789-237 HUMAN PRESCRIPTION DRUG Acetazolamide Acetazolamide TABLET ORAL 20220310 N/A ANDA ANDA211556 PD-Rx Pharmaceuticals, Inc. ACETAZOLAMIDE 250 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (72789-237-01)
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