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 60 条，共 3 页，当前第 2 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
71335-2457-6 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/1 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-6)
71335-2496-4 71335-2496 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20240916 N/A ANDA ANDA216800 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2496-4)
71335-2496-5 71335-2496 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20240916 N/A ANDA ANDA216800 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2496-5)
71335-2496-6 71335-2496 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20240916 N/A ANDA ANDA216800 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2496-6)
50090-7349-0 50090-7349 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20241016 N/A ANDA ANDA216800 A-S Medication Solutions BUPROPION HYDROCHLORIDE 100 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7349-0)
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)
50090-7423-0 50090-7423 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 (50090-7423-0)
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)
71335-2457-7 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 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-7)
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)
71335-2400-1 71335-2400 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20240613 N/A ANDA ANDA216800 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 200 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2400-1)
71335-2400-2 71335-2400 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20240613 N/A ANDA ANDA216800 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 200 mg/1 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2400-2)
71335-2400-3 71335-2400 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20240613 N/A ANDA ANDA216800 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 200 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2400-3)
71335-2400-4 71335-2400 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20240613 N/A ANDA ANDA216800 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 200 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2400-4)
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)
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