Lupin’s Aurangabad facility gets EIR from USFDA

Lupin’s Aurangabad facility gets EIR from USFDA

by admin- Monday, August 5th, 2019 03:54:57 PM

Pharma main Lupin has announced the receipt of the Establishment Inspection Report (EIR) from the USFDA for its Aurangabad facility. The facility became inspected by means of the USFDA between May 6, 2019 and May 15, 2019.

Lupin’s Aurangabad facility is concerned inside the manufacture of Oral Solid Dosage, Oral Liquid and Powder for Oral Suspension merchandise for the USA Market, WHO/Global Institution markets and the India marketplace.

News Updates