USFDA gives approval to Aleor for Lidocaine & Prilocaine cream

Lidocaine and prilocaine cream is indicated as a topical anaesthetic

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USFDA
Picture: Pixabay

Last Updated on April 13, 2022 by The Health Master

Alembic Pharmaceuticals Limited‘s wholly owned subsidiary, Aleor Dermaceuticals Limited (Aleor) has received final approval from the US Food & Drug Administration (FDA) for its Abbreviated New Drug Application (ANDA) for lidocaine and prilocaine cream USP, 2.5%/2.5%.

The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD) Emla cream, 2.5%/2.5%, of Teva Branded Pharmaceutical Products R&D, Inc.

Lidocaine 2.5% and prilocaine 2.5% cream (a eutectic mixture of lidocaine 2.5% and prilocaine 2.5%) is indicated as a topical anaesthetic for use on normal intact skin for local analgesia and genital mucous membranes for superficial minor surgery.

And as pre-treatment for infiltration anaesthesia. Lidocaine 2.5% and prilocaine 2.5% cream is not recommended in any clinical situation when penetration or migration beyond the tympanic membrane into the middle ear is possible because of the ototoxic effects observed in animal studies.

Lidocaine and prilocaine cream USP, 2.5%/2.5% has an estimated market size of US$ 29 million for twelve months ending December 2021 according to IQVIA. Alembic has received a cumulative total of 163 ANDA approvals (140 final approvals and 23 tentative approvals) from USFDA.

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