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Aurobindo Receives FDA Approval for Diclofenac Sodium Topical Solution USP, 2% w/w

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 : 

  • The treatment of the pain of osteoarthritis of the knee(s).