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
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)
82009-052-05 82009-052 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride XL Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20230707 N/A ANDA ANDA090693 Quallent Pharmaceuticals Health LLC BUPROPION HYDROCHLORIDE 300 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (82009-052-05)
50268-133-13 50268-133 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20250305 N/A ANDA ANDA090693 AvPAK BUPROPION HYDROCHLORIDE 150 mg/1 30 BLISTER PACK in 1 BOX (50268-133-13) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-133-11)
68180-319-02 68180-319 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride XL 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)
68180-319-06 68180-319 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride XL Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20170614 N/A ANDA ANDA090693 Lupin Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-319-06)
68180-319-09 68180-319 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride XL 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)
0904-7469-04 0904-7469 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride XL Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20241007 N/A ANDA ANDA090693 Major Pharmaceuticals BUPROPION HYDROCHLORIDE 300 mg/1 30 BLISTER PACK in 1 CARTON (0904-7469-04) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
60687-782-01 60687-782 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20240115 N/A ANDA ANDA090693 American Health Packaging BUPROPION HYDROCHLORIDE 150 mg/1 100 BLISTER PACK in 1 CARTON (60687-782-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-782-11)
50268-134-13 50268-134 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20250305 N/A ANDA ANDA090693 AvPAK BUPROPION HYDROCHLORIDE 300 mg/1 30 BLISTER PACK in 1 BOX (50268-134-13) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-134-11)
68180-320-02 68180-320 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride XL 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)
68180-320-06 68180-320 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride XL 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 XL 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)
68071-3559-9 68071-3559 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20240109 N/A ANDA ANDA090693 NuCare Pharmaceuticals,Inc. BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3559-9)
50090-6789-0 50090-6789 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20231031 N/A ANDA ANDA090693 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6789-0)
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