Vadodara: Drugmaker Alembic Pharma has recently announced that the Company has received Establishment Inspection Report (EIR) from US Food and Drug Administration (USFDA) for its Oncology Injectable Formulation Facility at Panelav.
The facility was inspected from 4 th October, 2022 to 14th October, 2022.
“This is to inform 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 our Oncology Injectable Formulation Facility at Panelav during the period from 4th October, 2022 to 14th October, 2022,” Alembic Pharma stated in a BSE filing.
were filed with USFDA. The Company had also started receiving ANDA approval
manufactured at this facility,” the company further stated.
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Medical Dialogues had earlier reported that the United States Food and Drug Administration (USFDA) had issued a Form 483 with 4 procedural observations after an inspection of the Panelav facility. An FDA Form 483 is issued to firm management at the conclusion of an inspection when an investigator(s) has observed any conditions that in their judgment may constitute violations of the Food Drug and Cosmetic (FD&C) Act and related Acts.
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Alembic Pharmaceuticals Limited is a vertically integrated research and development pharmaceutical company headquartered in Gujarat. It is involved in manufacturing and marketing India Formulations, International Generics, and Active Pharmaceutical Ingredients with vertical integration capabilities. Products under International Generics are manufactured across our world-class facilities in Panelav, Karkhadi, and Jarod in Gujarat. Under this vertical, the company also has R&D facilities in Vadodara (Gujarat), Hyderabad (Telangana), and New Jersey (USA).
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