Express Pharma

Aleor Dermaceuticals gets USFDA approval for Diclofenac Sodium Topical Gel

It is indicated for the topical treatment of actinic keratoses

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Alembic Pharmaceuticals announced that its wholly owned subsidiary, Aleor Dermaceuticals has received final approval from the US Food & Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) for Diclofenac Sodium Topical Gel, 3%.The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD) Solaraze Topical Gel, 3%, of Fougera Pharmaceuticals. (Fougera). Diclofenac Sodium Topical Gel, 3% is indicated for the topical treatment of actinic keratoses. Sun avoidance is indicated during therapy.

Diclofenac Sodium Topical Gel, 3% has an estimated market size of $10 million for twelve months ending March 2022 according to IQVIA.

Alembic has received a cumulative total of 169 ANDA approvals (145 final approvals and 24 tentative approvals) from USFDA.

 

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