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=ANDA090693"
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
68180-320-06 68180-320 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20170614 N/A ANDA ANDA090693 Lupin Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-320-06)
68180-320-09 68180-320 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20170614 N/A ANDA ANDA090693 Lupin Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 300 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-320-09)
68180-319-09 68180-319 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20170614 N/A ANDA ANDA090693 Lupin Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-319-09)
68180-319-02 68180-319 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20170614 N/A ANDA ANDA090693 Lupin Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 150 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-319-02)
68180-320-02 68180-320 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20170614 N/A ANDA ANDA090693 Lupin Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 300 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-320-02)
50090-4747-0 50090-4747 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20191122 N/A ANDA ANDA090693 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4747-0)
50090-4747-1 50090-4747 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20191122 N/A ANDA ANDA090693 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4747-1)
50090-4747-2 50090-4747 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20191122 N/A ANDA ANDA090693 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4747-2)
50090-4749-0 50090-4749 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20191122 N/A ANDA ANDA090693 A-S Medication Solutions BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4749-0)
50090-4749-1 50090-4749 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20191122 N/A ANDA ANDA090693 A-S Medication Solutions BUPROPION HYDROCHLORIDE 300 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4749-1)
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