Aquestive offers vertically integrated development and production capabilities, spanning product formulation to final product packaging. With expertise in pharmaceutical and over-the-counter product development, tech transfer, scale-up, manufacturing, and packaging, we support both small and large-scale solutions. Our FDA-approved facilities in Portage, Indiana, equipped with 34,400 square feet of storage, enable us to seamlessly support customers from packaging to distribution, providing a fully integrated CDMO platform for customized solutions.
With over 2 billion doses produced and packaged, Aquestive Therapeutics is the undisputed leader in developing and delivering medications via film, using our PharmFilm technology. Our PharmFilm technology is an alternative to more invasive drug administration methods such as injection, rectal and nasal applications. Our film enables patients and customers to experience easy, convenient dosing of their critical medication and their over-the-counter products. Building on our success, Aquestive has established a robust portfolio of transformative PharmFilm products, which have already been licensed and are sold across six continents.
In addition to our extensive manufacturing and primary packaging expertise, Aquestive has comprehensive secondary packaging capabilities to support both pharmaceutical and over-the-counter products. For pharmaceutical products, Aquestive offers DSCSA-compliant serialization that follows the latest FDA Drug Supply Chain Security Act requirements for product traceability. Our secondary packaging equipment produces the highest quality finished product with both speed and accuracy. Whether you require the packaging of a high-volume or a small-volume product, our project management and operations experts will provide appropriate solutions for your product.
Aquestive has solution mixing experience focused on the production of both pharmaceutical and over-the-counter products for a variety of vendors. With different mix platforms and different sized mix tanks from 12 gallons to 500 liters, we can seamlessly manufacture products from pilot scale to commercial scale. Our expertise in mixing products enables us to maintain the homogeneity of all ingredients throughout the mixing process. Beginning with analytical and formulation development, our team’s experts complete all phases of production within our FDA-approved facilities, while following the strictest FDA requirements to achieve the desired therapeutic effect.
