About Us

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55+ years in business

Clinical Support

Pharmacists and scientists available

We are a state-of-the-art, FDA registered 503B outsourcing facility that provides healthcare practitioners, clinics, hospitals, group purchasing organizations, and other provider networks with the highest-quality manufactured medications.  We also have a 503A compounding pharmacy, which gives us the unique ability to provide our healthcare partners and their patients with nearly any custom manufactured or compounded medication they need.

We were founded in 1965 as a small community pharmacy, serving the local Dallas-Ft. Worth area.  We started working with general practitioners, urologists, and OB-GYNs and quickly became known for our hormone medications.  Soon, we were one of the leading suppliers of implantable subcutaneous hormone pellets and innovated the modern automated pellet manufacturing process.  In 2015, we became one of the earliest independently owned facilities to register with the FDA as a 503B outsourcing facility, and in 2019, we moved into our current facility in order to increase our manufacturing capacity and support our growing team of professionals.

Today, as one of the leaders in our industry, we continue to look for opportunities to serve our healthcare partners.  Whether we are compounding a routine prescription or having our team of research and development pharmacists create a new 503B product, our commitment is to provide our partners and the healthcare system in general with superior quality, service, and innovation.

Carie Boyd's professional practitioners developing high quality solutions in their brand new laboratories

Quality at the forefront

Our quality assurance and quality control exceed the industry’s requirements and standards.


We’re here for you

Providing our customers with unparalleled, superior service is fundamental to who we are.

customer service, expert practitioner solving concerns to customer

Innovation is a must

Our ongoing commitment to innovating new products and processes has made us a thought-leader in the healthcare industry.

What is a 503B Outsourcing Facility?

Outsourcing facilities like Carie Boyd have registered with the FDA pursuant to Section 503B of the Federal Food, Drug, and Cosmetic Act. They manufacture medications for administration or use in healthcare facilities and providers’ offices. These manufactured medications are distributed by the outsourcing facility that made them directly to the healthcare facility or provider without a prescription.

How is it done?

As an outsourcing facility, Carie Boyd manufactures medications under Current Good Manufacturing Practice requirements. These requirements mandate the use of certain cleanroom classifications, manufacturing equipment, monitoring systems, quality management systems, raw material controls, and other protocols and processes. This helps ensure that 503B products are produced under the same conditions and pursuant to the same standards as commercially available medications. It takes teams of pharmacists, scientists, and technicians to operate outsourcing facilities like ours.

Why is it important?

Carie Boyd and other outsourcing facilities fill important needs within the pharmaceutical supply chain. They provide safe and effective medications that are not commercially available but are nonetheless needed by certain segments of the population. Additionally, outsourcing facilities help to ensure a steady supply of medication for our nation’s healthcare system by manufacturing medications that have been made commercially available but are on the FDA’s drug shortages list.

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