Alembic Pharmaceuticals has informed the exchange that the Company has received Establishment Inspection Report (EIR) from US Food and Drug Administration (USFDA) for the inspection carried out by them at its Solid Oral Formulation Facility (F-4) at Jarod, Vadodara during the period from 8th December, 2022 to 16th December, 2022. This was pre-approval inspection to cover our Solid Oral drug products for which ANDAs were filed with USFDA. The Company had also started receiving approvals manufactured at this facility. Alembic has a total of five drug product manufacturing facilities and two drug substance manufacturing facilities. All these facilities are inspected and accepted by USFDA.
The above information is a part of company’s filings submitted to BSE.
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