Jubilant Pharmova gets USFDA nod for Spokane facility's Line 3
Jubilant Pharmova's subsidiary, Jubilant HollisterStier LLC, received USFDA approval for commercial batch manufacturing on its new Isolator-based fill and finish line, Line 3, at its Spokane, U.S.A. facility. This approval allows for the production of the first product on this line.
The approval of a new manufacturing line for commercial batch production is a significant operational milestone that can enhance the company's manufacturing capacity and revenue potential in the contract manufacturing segment.
The USFDA approval for a new manufacturing line signifies operational progress and regulatory compliance, which is positive for the company's contract manufacturing business.
Jubilant Pharmova Limited announced on August 23, 2026, that the U.S. Food and Drug Administration (USFDA) has approved the commercial batch manufacturing of the first product on Line 3 at its Jubilant HollisterStier LLC (JHS) contract manufacturing facility in Spokane, Washington, U.S.A.
Line 3 is an Isolator-based fill and finish line. Jubilant HollisterStier LLC is a subsidiary of Jubilant Pharma Holding Inc., which is itself a subsidiary of Jubilant Pharma Limited, Singapore, a wholly owned subsidiary of Jubilant Pharmova Limited.
Jubilant HollisterStier is a contract manufacturer of sterile injectables and ophthalmics, serving the pharmaceutical and biopharmaceutical industries with facilities in North America. Jubilant Pharma Limited is an integrated global pharmaceutical company with businesses in Radiopharmaceuticals, Allergy Immunotherapy, Contract Manufacturing of Sterile Injectables and Non-sterile products, and Solid Dosage Formulations. Jubilant Pharmova Limited operates globally in Radiopharma, Allergy Immunotherapy, Contract Development and Manufacturing of sterile injectables, Contract Research Development and Manufacturing, Generics, and Proprietary Novel Drugs.
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