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"
符合检索条件的记录共 35 条，共 2 页，当前第 1 页 ，可点击列名称排序
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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)
60687-793-21 60687-793 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20240115 N/A ANDA ANDA090693 American Health Packaging BUPROPION HYDROCHLORIDE 300 mg/1 30 BLISTER PACK in 1 CARTON (60687-793-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-793-11)
68788-8677-1 68788-8677 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20240523 N/A ANDA ANDA090693 Preferred Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 300 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8677-1)
68788-8677-3 68788-8677 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20240523 N/A ANDA ANDA090693 Preferred Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8677-3)
68788-8677-6 68788-8677 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20240523 N/A ANDA ANDA090693 Preferred Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 300 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8677-6)
68788-8677-8 68788-8677 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20240523 N/A ANDA ANDA090693 Preferred Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 300 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8677-8)
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)
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)
70518-2022-2 70518-2022 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20250706 N/A ANDA ANDA090693 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2022-2)
50090-7602-0 50090-7602 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride XL Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20250714 N/A ANDA ANDA090693 A-S Medication Solutions BUPROPION HYDROCHLORIDE 300 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7602-0)
0904-7505-04 0904-7505 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride XL Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20241125 N/A ANDA ANDA090693 Major Pharmaceuticals BUPROPION HYDROCHLORIDE 150 mg/1 30 BLISTER PACK in 1 CARTON (0904-7505-04) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
68788-8677-9 68788-8677 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20240523 N/A ANDA ANDA090693 Preferred Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 300 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8677-9)
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)
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)
0904-7505-61 0904-7505 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride XL Bupropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20241125 N/A ANDA ANDA090693 Major Pharmaceuticals BUPROPION HYDROCHLORIDE 150 mg/1 100 BLISTER PACK in 1 CARTON (0904-7505-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
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