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About Us

Our Story

Medi-Fare Drug prides itself on being one of the first compounding pharmacies to voluntarily register with the FDA as a 503B Outsourcing Facility.

What began over 30 years ago as a retail pharmacy serving local patients and hospitals has evolved into a business that, for the last decade, has focused solely on providing sterile medications to hospitals, physicians, and clinics.

Medi-Fare Drug is committed to providing our partners with products of the highest quality and excellence in customer service.

We are driven by values

Medi-Fare Drug has a custom designed and constructed state of the art clean room that is specifically suited for the cGMP production of a wide variety of sterile products including admixtures, ophthalmics, and diagnostic agents. We also prepare a variety of specialized drug shortage medications, all of which can be multi-dose, unit-dose, or preservative-free.

Our meticulous attention to detail, from environmental testing and cleanroom sanitization, to real-time particulate monitoring ensures sterility is maintained and that quality is by design. Medi-Fare is excited to have recently expanded its facility by constructing a 335 square foot vault in order to increase product volume, which was certified by the DEA in January 2023.

All of our preparations undergo rigorous testing by third-party, independent laboratories, evaluating a wide range of criteria like potency, sterility, pyrogens, stability, and fungi.


Medi-Fare Drug is committed to providing our customers with quality products and exceptional customer service.

  • cGMP validated processes, equipment, and facility
  • Using only tested materials from FDA-registered facilities
  • Trained, experienced, and tested staff
  • Checking and rechecking of preparations
  • Quality control unit oversight, documentation, and testing
  • Quality control unit oversight, documentation, and testing


Medi-Fare Drug has all the processes in place to ensure product safety, including:

  • Fourteen years of pharmacy-based compounding experience
  • State of the art cleanroom
  • Ongoing staff training and education
  • Environmental and personnel testing
  • Process validation
  • Third-party, rigorous API and end-product testing
  • Certificate of analysis verification