Aurobindo Receives FDA Approval for Diclofenac Sodium Topical Solution USP, 2% w/w
Published: February 03, 2023
Published: February 03, 2023
East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Diclofenac Sodium Topical Solution USP, 2% w/w. Aurobindo Pharma’s Diclofenac Sodium Topical Solution, are an AB-rated generic equivalent to the reference listed drug (RLD), Pennsaid® Topical Solution manufactured by Horizon Therapeutics.
Diclofenac Sodium Topical Solution are indicated for :