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=ANDA076913"
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
67296-1505-6 67296-1505 HUMAN PRESCRIPTION DRUG Prednisolone Sodium Phosphate Prednisolone Sodium Phosphate SOLUTION ORAL 20050425 N/A ANDA ANDA076913 RedPharm Drug, Inc. PREDNISOLONE SODIUM PHOSPHATE 15 mg/5mL 60 mL in 1 BOTTLE (67296-1505-6)
50090-1582-0 50090-1582 HUMAN PRESCRIPTION DRUG Prednisolone Sodium Phosphate Prednisolone Sodium Phosphate SOLUTION ORAL 20141229 N/A ANDA ANDA076913 A-S Medication Solutions PREDNISOLONE SODIUM PHOSPHATE 15 mg/5mL 237 mL in 1 BOTTLE (50090-1582-0)
68788-7708-2 68788-7708 HUMAN PRESCRIPTION DRUG Prednisolone Sodium Phosphate Prednisolone Sodium Phosphate SOLUTION ORAL 20200601 N/A ANDA ANDA076913 Preferred Pharmaceuticals, Inc. PREDNISOLONE SODIUM PHOSPHATE 15 mg/5mL 237 mL in 1 BOTTLE (68788-7708-2)
63187-215-64 63187-215 HUMAN PRESCRIPTION DRUG Prednisolone Sodium Phosphate Prednisolone Sodium Phosphate SOLUTION ORAL 20140901 N/A ANDA ANDA076913 Proficient Rx LP PREDNISOLONE SODIUM PHOSPHATE 15 mg/5mL 240 mL in 1 BOTTLE (63187-215-64)
0121-0759-08 0121-0759 HUMAN PRESCRIPTION DRUG Prednisolone Sodium Phosphate Prednisolone Sodium Phosphate SOLUTION ORAL 20050425 N/A ANDA ANDA076913 PAI Holdings, LLC dba PAI Pharma PREDNISOLONE SODIUM PHOSPHATE 15 mg/5mL 237 mL in 1 BOTTLE (0121-0759-08)
0121-4759-50 0121-4759 HUMAN PRESCRIPTION DRUG Prednisolone Sodium Phosphate Prednisolone Sodium Phosphate SOLUTION ORAL 20240322 N/A ANDA ANDA076913 PAI Holdings, LLC dba PAI Pharma PREDNISOLONE SODIUM PHOSPHATE 15 mg/5mL 5 TRAY in 1 CASE (0121-4759-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-4759-05)
70518-4524-0 70518-4524 HUMAN PRESCRIPTION DRUG Prednisolone Sodium Phosphate Prednisolone Sodium Phosphate SOLUTION ORAL 20251128 N/A ANDA ANDA076913 REMEDYREPACK INC. PREDNISOLONE SODIUM PHOSPHATE 15 mg/5mL 2 CUP in 1 BOX (70518-4524-0) / 25 mL in 1 CUP (70518-4524-1)
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