Lupin’s Pithampur Unit-3 receives EIR from USFDA
December 10, 2018 | Monday | News
The inspection at the site was conducted between June 12, 2017 and June 16, 2017. This was a Pre-approval inspection for Albuterol Sulfate Inhalation product
Pharma major Lupin has announced the receipt of the Establishment Inspection Report (EIR) for its Pithampur (Unit 3) facility.
The inspection at the site was conducted between June 12, 2017 and June 16, 2017. This was a Pre-approval inspection for Albuterol Sulfate Inhalation product.
Commenting on the development, Nilesh Gupta, Managing Director, Lupin said, “The receipt of the EIR for our Pithampur Unit 3 is an encouraging development. This is a validation of our commitment to maintain the highest standards in quality and compliance across our facilities.”
Lupin’s Pithampur (Unit 3) facility manufactures Dermatological Products, Dry Product Inhalers and Metered Dose Inhalers.
