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Aleor’s ANDA for treatment of cutaneous candidiasis gets USFDA nod April 01, 2021 ANDA is for Nystatin and Triamcinolone Acetonide Cream USP to be marketed in US Alembic Pharmaceuticals Limited’s joint venture Aleor Dermaceuticals Limited (Aleor) has received final approval from the US drug regulator, US Food & Drug Administration (USFDA), for an Abbreviated New Drug Application (ANDA) for Nystatin and Triamcinolone Acetonide Cream USP, the company informed. Aleor is a 60:40 joint venture between Alembic Pharmaceuticals Limited and Orbicular Pharmaceutical Technologies Pvt Ltd (Orbicular) focused on commercialising dermatology products globally. The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD), Nystatin and Triamcinolone Acetonide Cream USP, 100,000 units/gram and 1 mg/gram, of Taro Pharmaceuticals U.S.A. Inc, an official statement said here.

Alembic pharmaceuticalsAleor dermaceuticals limitedOrbicular pharmaceutical technologies pvt ltdUs food drug administrationTaro pharmaceuticals united statesAlembic pharmaceuticals limitedDrug administrationAbbreviated new drug applicationTriamcinolone acetonide creamTaro pharmaceuticals unitedஅலெம்பிக் மருந்துகள்அலெவ்ர் தோல் வரையறுக்கப்பட்டவைடாரோ மருந்துகள் ஒன்றுபட்டது மாநிலங்களில்அலெம்பிக் மருந்துகள் வரையறுக்கப்பட்டவைடாரோ மருந்துகள் ஒன்றுபட்டது