On 1st February 2021, AET Pharma US Inc, part of TIEFENBACHER GROUP, received FDA approval of the Abbreviated New Drug Application (ANDA) for Posaconazole 100 mg Delayed-Release Tablets. This is another milestone for TIEFENBACHER GROUP in further strengthening its product portfolio in the United States. The US launch of Posaconazole will proceed in close cooperation with our experienced distribution partner, Lupin Pharmaceuticals Inc. With the market entry of Posaconazole, we look forward to increasing availability and ensuring affordability of this treatment for American patients.

The product has been developed by and is manufactured at TIEFENBACHER LABORATORIES in Hyderabad, India, and has already been successfully launched in the European Union and in Australia. The registration dossier is currently under filing in several additional international markets.

For more information, please contact TIEFENBACHER PHARMACEUTICALS: info@aet.eu