Lupin has informed that it has enclosed a Press Release on 25th August 2020 as regards receipt of U.S. FDA approval for the Company’s Albuterol Sulfate Inhalation Aerosol, 90 mcg (base)/actuation, a generic version of ProAir® HFA. Generic Albuterol Sulphate MDI will be manufactured at the Company’s Indore (Unit III) facility in India. This may be considered as a disclosure pursuant to Regulation 30 of the SEBI (Listing Obligations and Disclosure Requirements) Regulations, 2015.
The above information is a part of company’s filings submitted to BSE.