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=ANDA075356"
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
60505-0101-1 60505-0101 HUMAN PRESCRIPTION DRUG PAROXETINE paroxetine hydrochloride TABLET, FILM COATED ORAL 20030908 N/A ANDA ANDA075356 Apotex Corp. PAROXETINE HYDROCHLORIDE ANHYDROUS 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (60505-0101-1)
60505-0101-2 60505-0101 HUMAN PRESCRIPTION DRUG PAROXETINE paroxetine hydrochloride TABLET, FILM COATED ORAL 20030908 N/A ANDA ANDA075356 Apotex Corp. PAROXETINE HYDROCHLORIDE ANHYDROUS 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (60505-0101-2)
60505-0101-4 60505-0101 HUMAN PRESCRIPTION DRUG PAROXETINE paroxetine hydrochloride TABLET, FILM COATED ORAL 20030908 N/A ANDA ANDA075356 Apotex Corp. PAROXETINE HYDROCHLORIDE ANHYDROUS 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (60505-0101-4)
60505-0084-4 60505-0084 HUMAN PRESCRIPTION DRUG PAROXETINE paroxetine hydrochloride TABLET, FILM COATED ORAL 20030908 N/A ANDA ANDA075356 Apotex Corp. PAROXETINE HYDROCHLORIDE ANHYDROUS 30 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (60505-0084-4)
60429-736-10 60429-736 HUMAN PRESCRIPTION DRUG PAROXETINE paroxetine hydrochloride TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA075356 Golden State Medical Supply, Inc. PAROXETINE HYDROCHLORIDE ANHYDROUS 30 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (60429-736-10)
60429-736-30 60429-736 HUMAN PRESCRIPTION DRUG PAROXETINE paroxetine hydrochloride TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA075356 Golden State Medical Supply, Inc. PAROXETINE HYDROCHLORIDE ANHYDROUS 30 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (60429-736-30)
60429-736-90 60429-736 HUMAN PRESCRIPTION DRUG PAROXETINE paroxetine hydrochloride TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA075356 Golden State Medical Supply, Inc. PAROXETINE HYDROCHLORIDE ANHYDROUS 30 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (60429-736-90)
60429-737-10 60429-737 HUMAN PRESCRIPTION DRUG PAROXETINE paroxetine hydrochloride TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA075356 Golden State Medical Supply, Inc. PAROXETINE HYDROCHLORIDE ANHYDROUS 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (60429-737-10)
60429-737-30 60429-737 HUMAN PRESCRIPTION DRUG PAROXETINE paroxetine hydrochloride TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA075356 Golden State Medical Supply, Inc. PAROXETINE HYDROCHLORIDE ANHYDROUS 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (60429-737-30)
60429-737-90 60429-737 HUMAN PRESCRIPTION DRUG PAROXETINE paroxetine hydrochloride TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA075356 Golden State Medical Supply, Inc. PAROXETINE HYDROCHLORIDE ANHYDROUS 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (60429-737-90)
60505-0083-1 60505-0083 HUMAN PRESCRIPTION DRUG PAROXETINE paroxetine hydrochloride TABLET, FILM COATED ORAL 20030908 N/A ANDA ANDA075356 Apotex Corp. PAROXETINE HYDROCHLORIDE ANHYDROUS 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (60505-0083-1)
60505-0083-2 60505-0083 HUMAN PRESCRIPTION DRUG PAROXETINE paroxetine hydrochloride TABLET, FILM COATED ORAL 20030908 N/A ANDA ANDA075356 Apotex Corp. PAROXETINE HYDROCHLORIDE ANHYDROUS 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (60505-0083-2)
60505-0083-4 60505-0083 HUMAN PRESCRIPTION DRUG PAROXETINE paroxetine hydrochloride TABLET, FILM COATED ORAL 20030908 N/A ANDA ANDA075356 Apotex Corp. PAROXETINE HYDROCHLORIDE ANHYDROUS 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (60505-0083-4)
60505-0097-2 60505-0097 HUMAN PRESCRIPTION DRUG PAROXETINE paroxetine hydrochloride TABLET, FILM COATED ORAL 20030908 N/A ANDA ANDA075356 Apotex Corp. PAROXETINE HYDROCHLORIDE ANHYDROUS 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (60505-0097-2)
61919-322-30 61919-322 HUMAN PRESCRIPTION DRUG PAROXETINE PAROXETINE TABLET, FILM COATED ORAL 20150101 N/A ANDA ANDA075356 DIRECT RX PAROXETINE HYDROCHLORIDE ANHYDROUS 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (61919-322-30)
60505-0097-1 60505-0097 HUMAN PRESCRIPTION DRUG PAROXETINE paroxetine hydrochloride TABLET, FILM COATED ORAL 20030908 N/A ANDA ANDA075356 Apotex Corp. PAROXETINE HYDROCHLORIDE ANHYDROUS 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (60505-0097-1)
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