BROMOTAK

Bromfenac Sodium eq. to Bromfenac 0.09% w/v, Moxifloxacin HCI I.P. to eq. to Moxifloxacin 0.5% w/v Bezalkonium Chloride Solution I.P. 0.02% v/v

The power to be on control of critical of ophthalmic Probabilities It is most powerful derivatives of fourth generation with bacterial activity against gram positive & gram negative It is more effective due to more time contacted to the tear film *Bromfenac is a non-steroidal anti-inflammatory drug.

It prevents prostaglandin H Synthesis that causes papillary miosis. It decreases prostaglandin production by inhibiting cyclooxygenase 1 and 2, thereby inhibiting the inflammatory process. Due to the addition of the bromine group to its molecule, bromfenac has more affinity for lipids.