Niagen Bioscience, Inc. (NASDAQ:NAGE), the global authority on NAD+ (nicotinamide adenine dinucleotide) with a focus on the science of healthy aging, today announced a new partnership with Olympia Pharmaceuticals, a state-of-the-art U.S. FDA-registered 503B outsourcing facility, to compound and distribute pharmaceutical-grade Niagen® (patented nicotinamide riboside, NR) for the Company's Niagen Plus™ intravenous and injectable products. Olympia Pharmaceuticals joins Wells Pharma of Houston, diversifying the Company's 503B network and supply chain capabilities to support continued growth across its clinic footprint and expand access to the Company's innovative Niagen Plus product pipeline.

"We anticipate that Olympia will play an important role in meeting the growing demand for Niagen IV and Niagen injections," said Rob Fried, Chief Executive Officer of Niagen Bioscience.

Under its Niagen Plus product portfolio, Niagen Bioscience developed its next-generation intravenous formulation of pharmaceutical-grade Niagen designed to support healthy aging and longevity at the cellular level. Compared to traditional NAD+ IV, the aqueous-based Niagen IV supports faster infusions and elevates NAD+ levels higher without the severe side effects of NAD+ IV (Reyna et al., 2026; Hawkins et al., 2024). Niagen Bioscience recently reported the expansion of its NAD+ precursor intellectual property (IP), with a newly granted patent covering methods of use for Niagen and its derivatives in IV and injectable formulations.

"We are honored to partner with Niagen Bioscience, a company that has set the standard for quality and scientific rigor in the NAD+ category," said Dr. Mark Mikhael, PharmD, Chief Executive Officer of Olympia Pharmaceuticals. "Their leadership in pharmaceutical-grade Niagen and disciplined approach to innovation make them an exceptional partner, and we are proud to support growing demand for Niagen Plus with the manufacturing quality and reliability this market requires."

Olympia Pharmaceuticals is a state-of-the-art 503B facility serving providers and patients nationwide, distinguished by its focus on quality, regulatory excellence, and premium compounded medications. Licensed across 49 states, Olympia follows cGMP (Current Good Manufacturing Practices), the same guidelines as pharmaceutical manufacturers, supports its operations with dedicated Quality and Compliance teams, and conducts rigorous third-party testing to help ensure the consistent delivery of high-quality pharmaceutical solutions.