Alembic Pharmaceuticals gets USFDA approval for Dapsone Gel, 5%

Dapsone Gel is indicated for the topical treatment of acne vulgaris

Alembic Pharmaceuticals has received final approval from the US Food & Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) Dapsone Gel, 5%.

Dapsone Gel is indicated for the topical treatment of acne vulgaris.

The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD), Aczone Gel, 5%, of Almirall, LLC.

Alembic has a cumulative total of 244 ANDA approvals (224 final approvals and 20 tentative approvals) from USFDA.

acne vulgarisAlembic PharmaceuticalsANDA approvalDapsone gelUSFDA
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