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=ANDA216800"
符合检索条件的记录共 61 条，共 4 页，当前第 3 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
71335-2457-8 71335-2457 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20240820 N/A ANDA ANDA216800 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 150 mg/1 56 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-8)
71335-2457-9 71335-2457 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20240820 N/A ANDA ANDA216800 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 150 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-9)
50090-7422-0 50090-7422 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20241028 N/A ANDA ANDA216800 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7422-0)
50090-7422-1 50090-7422 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20241028 N/A ANDA ANDA216800 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7422-1)
50090-7422-2 50090-7422 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20241028 N/A ANDA ANDA216800 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7422-2)
50090-7422-3 50090-7422 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20241028 N/A ANDA ANDA216800 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7422-3)
70518-4081-1 70518-4081 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20240926 N/A ANDA ANDA216800 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4081-1)
70518-4081-2 70518-4081 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20250701 N/A ANDA ANDA216800 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4081-2)
70518-4081-3 70518-4081 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20250701 N/A ANDA ANDA216800 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4081-3)
70518-4081-4 70518-4081 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20250827 N/A ANDA ANDA216800 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4081-4)
68788-8769-1 68788-8769 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20241119 N/A ANDA ANDA216800 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 150 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-1)
68788-8769-2 68788-8769 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20241119 N/A ANDA ANDA216800 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 150 mg/1 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-2)
68788-8769-3 68788-8769 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20241119 N/A ANDA ANDA216800 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-3)
68788-8769-6 68788-8769 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20241119 N/A ANDA ANDA216800 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-6)
68788-8769-8 68788-8769 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20241119 N/A ANDA ANDA216800 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 150 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-8)
68788-8769-9 68788-8769 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20241119 N/A ANDA ANDA216800 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-9)
31722-068-01 31722-068 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230531 N/A ANDA ANDA216800 Camber Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 200 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-01)
31722-068-05 31722-068 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230531 N/A ANDA ANDA216800 Camber Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 200 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-05)
31722-068-60 31722-068 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230531 N/A ANDA ANDA216800 Camber Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 200 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-60)
31722-068-90 31722-068 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230531 N/A ANDA ANDA216800 Camber Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 200 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-90)
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