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=ANDA202413"
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
71335-3121-3 71335-3121 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260413 N/A ANDA ANDA202413 Bryant Ranch Prepack IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-3121-3)
71335-3121-4 71335-3121 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260413 N/A ANDA ANDA202413 Bryant Ranch Prepack IBUPROFEN 600 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71335-3121-4)
71335-3121-5 71335-3121 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260413 N/A ANDA ANDA202413 Bryant Ranch Prepack IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-3121-5)
71335-3121-6 71335-3121 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260413 N/A ANDA ANDA202413 Bryant Ranch Prepack IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-3121-6)
71335-3121-7 71335-3121 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260413 N/A ANDA ANDA202413 Bryant Ranch Prepack IBUPROFEN 600 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-3121-7)
50090-7905-0 50090-7905 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260216 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (50090-7905-0)
50090-7320-0 50090-7320 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241014 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-7320-0)
67296-2184-2 67296-2184 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240523 N/A ANDA ANDA202413 Redpharm Drug IBUPROFEN 400 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (67296-2184-2)
85509-2396-3 85509-2396 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250730 N/A ANDA ANDA202413 PHOENIX RX LLC IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (85509-2396-3)
85509-2396-6 85509-2396 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250730 N/A ANDA ANDA202413 PHOENIX RX LLC IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (85509-2396-6)
85509-2396-9 85509-2396 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250730 N/A ANDA ANDA202413 PHOENIX RX LLC IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (85509-2396-9)
62135-400-12 62135-400 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220810 N/A ANDA ANDA202413 Chartwell RX, LLC IBUPROFEN 400 mg/1 120 TABLET, FILM COATED in 1 PACKAGE (62135-400-12)
72789-565-15 72789-565 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260605 N/A ANDA ANDA202413 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-565-15)
72789-565-30 72789-565 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260416 N/A ANDA ANDA202413 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-565-30)
71335-3121-8 71335-3121 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260413 N/A ANDA ANDA202413 Bryant Ranch Prepack IBUPROFEN 600 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (71335-3121-8)
71335-3121-9 71335-3121 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260413 N/A ANDA ANDA202413 Bryant Ranch Prepack IBUPROFEN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-3121-9)
76420-848-05 76420-848 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-848-05)
76420-848-30 76420-848 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-848-30)
76420-848-60 76420-848 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-848-60)
76420-848-90 76420-848 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-848-90)
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