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Business Economy


Tagoor Laboratories receives DCGI license to manufacture Favipiravir API

Hyderabad, Oct 4 (UNI) Tagoor Laboratories Private Limited has received Drugs Controller General of India (DCGI) license to manufacture Favipiravir API.

The Active Pharmaceutical Ingredients (API) of an Anti-Viral Drug was approved by the DCGI for use in the treatment of mild to moderate COVID-19 cases.
The manufacturing facility located in West Godavari district of Andhra Pradesh has successfully completed Favipiravir development and is planning to enhance its production capabilities, a company release here said on Sunday.
The DCGI earlier approved the use of Favipiravir, an anti-viral drug used for treatment of influenza.
The drug, developed in Japan, is also used for the treatment of mild to moderate cases of Covid-19 in India.
Favipiravir is a broad spectrum anti-viral agent and selectively inhibits RNA polymerase of influenza virus and prevents viral replication.
Commenting on the receiving the license, Dr P Kasi Viswanadha Raju, Managing Director said, “Tagoor Laboratories is capable of producing the drug without having to depend on any imports, as all the complex intermediates are developed in-house.
The Company is aiming to manufacture Favipiravir in quantities sufficient to meet the growing domestic demand, which arose due to the pandemic.
Additionally, Tagoor Laboratories also manufactures and supplies Hydroxychloroquine sulphate, also used to treat COVID-19 symptoms.
Our manufacturing facility, approved by the WHO GMP, clocked an annual turnover of Rs 270 crore in the financial year 2019-2020, and is expected to make a Revenue of Rs 450 crore in the fiscal 2020-2021.
The Company has its R&D facility in Jeedimetla Industrial area in Hyderabad.”
Business Head Dr Mohanbabu Maradolla said “Tagoor Laboratories Private Limited is in talks with the top buyers in the domestic market and is also making collaborations with various Turkish, Iran, Egypt, and Russia partners to supply the Favipiravir API.”
UNI VV CS 1619
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