| abstract |
The invention discloses a levofloxacin lactate injection, which comprises 5-8 g of levofloxacin lactate, 3‐4 g of long-chain triglyceride per liter of injection, 2‐4 g of Tween, 5-6 g of sodium chloride, and ferrous gluconate 0.2‐. 0.4g, sodium citrate-sodium citrate buffer solution 400-600g, the balance is water for injection. The levofloxacin lactate injection overcomes the defects of poor solubility and poor stability, and has the characteristics of solubility and stability after being left for a long time, the color is not yellow, the clarity is in compliance with the regulations, the pH is not decreased, and the content is stable. Moreover, the preparation method is simple, easy to control, and has high promotion and application value. |