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=ANDA065162"
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
53002-1716-2 53002-1716 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium POWDER, FOR SUSPENSION ORAL 20181001 N/A ANDA ANDA065162 RPK Pharmaceuticals, Inc. AMOXICILLIN; CLAVULANATE POTASSIUM 600 mg/5mL; 42.9 mg/5mL 75 mL in 1 BOTTLE (53002-1716-2)
63187-857-75 63187-857 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium POWDER, FOR SUSPENSION ORAL 20190901 N/A ANDA ANDA065162 Proficient Rx LP AMOXICILLIN; CLAVULANATE POTASSIUM 600 mg/5mL; 42.9 mg/5mL 75 mL in 1 BOTTLE (63187-857-75)
53002-1716-1 53002-1716 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium POWDER, FOR SUSPENSION ORAL 20181001 N/A ANDA ANDA065162 RPK Pharmaceuticals, Inc. AMOXICILLIN; CLAVULANATE POTASSIUM 600 mg/5mL; 42.9 mg/5mL 200 mL in 1 BOTTLE (53002-1716-1)
63187-857-20 63187-857 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium POWDER, FOR SUSPENSION ORAL 20181101 N/A ANDA ANDA065162 Proficient Rx LP AMOXICILLIN; CLAVULANATE POTASSIUM 600 mg/5mL; 42.9 mg/5mL 200 mL in 1 BOTTLE (63187-857-20)
63187-857-12 63187-857 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium POWDER, FOR SUSPENSION ORAL 20170601 N/A ANDA ANDA065162 Proficient Rx LP AMOXICILLIN; CLAVULANATE POTASSIUM 600 mg/5mL; 42.9 mg/5mL 125 mL in 1 BOTTLE (63187-857-12)
0093-8675-78 0093-8675 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium POWDER, FOR SUSPENSION ORAL 20040923 N/A ANDA ANDA065162 Teva Pharmaceuticals USA, Inc. AMOXICILLIN; CLAVULANATE POTASSIUM 600 mg/5mL; 42.9 mg/5mL 75 mL in 1 BOTTLE (0093-8675-78)
0093-8675-74 0093-8675 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium POWDER, FOR SUSPENSION ORAL 20040923 N/A ANDA ANDA065162 Teva Pharmaceuticals USA, Inc. AMOXICILLIN; CLAVULANATE POTASSIUM 600 mg/5mL; 42.9 mg/5mL 200 mL in 1 BOTTLE (0093-8675-74)
0093-8675-75 0093-8675 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium POWDER, FOR SUSPENSION ORAL 20040923 N/A ANDA ANDA065162 Teva Pharmaceuticals USA, Inc. AMOXICILLIN; CLAVULANATE POTASSIUM 600 mg/5mL; 42.9 mg/5mL 125 mL in 1 BOTTLE (0093-8675-75)
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