Meeting All Your Oncological Veterinary Demands

FDA-registered 503B outsourcing provider of high quality medications and hospital-based services

  • We welcome your inspections of our facility
  • Excellent history of no patient adverse reactions to any of our compounded products
  • Exceptional competitive pricing
  • Stellar track record on the state and federal level audits and compliances
  • Our dedication to client satisfaction is reflected in our exemplary services

For Veterinarian

Our expertly trained pharmacists and friendly staff pride themselves on making sure your pharmacy experience exceeds expectations.


  • Required to register with each state board of pharmacy, DEA and FDA
  • Complies with cGMP regulations. Conducts 100% release testing on drug batches
  • 503B label standards with barcoding, ISMP-safe labeling features
  • Non-patient specific, with beyond use dating
  • Product available for office use

The difference between 503A and 503B

A great advantage of a 503B compounding pharmacy is the ability to make preparations in bulk without patient specific prescriptions, available for in office use.  This helps veterinarians that are struggling with drug shortages, price gouging, and sourcing difficult to find medications.  In fact, the FDA has encouraged hospitals to use a 503B compounding service to meet these specific needs. Read More

The main difference between 503B and 503A facilities, and a major practice of CGMP, is the requirement for every process to be validated in a 503B outsourcing facility.  Multiple batches must be made and submitted for testing and stability studies, before any new product can be brought to market.  Although production time frames may be prolonged, this certifies that batches made during normal production is dependable in quality and meets the standards set by the FDA and CGMP.  Testing and validation methods must also guarantee accuracy according to USP standards.


  • Complies with USP <795> and <797>
  • Regulated by State board of pharmacy
  • Not licensed or regulated by FDA
  • Require patient-specific prescriptions
  • No “office use”*
  • Limit on bulk compounding.  Restriction on compounding copies.


  • Complies with USP<795and <797and also
  • Complies with 21 CFR Part 210 & 211 (CGMP)
  • Regulated by FDA
  • Required by FDA to follow strict testing standards for sterility, potency, and endotoxins
  • Prescriptions are optional
  • Can compound for office use 
  • If shortage, can compound extra.  Manufacturers of sterile compounding.


Our expertly trained pharmacists and friendly staff pride themselves on making sure your pharmacy experience exceeds expectations.

Dependable Service & Technology

Our 503B Outsourcing Facility is located within our industry leading manufacturing campus, so we can use our quality, regulatory, and validation resources for sterile drug compounding. Our outsourcing division is regularly inspected by the FDA and operates certified clean rooms using current Good Manufacturing practices (cGMP). We have invested in the latest technology advancements, so you can be confident in our process, service, logistics, and uninterrupted supply chain. We are positioned to help your health care facility succeed.

We are a registered 503B outsourcing facility with certified clean rooms and two decades of experience complying with current Good Manufacturing Practice (cGMP).

List Of Medication

  • Asparaginase
  • Carboplatin
  • Chlorambucil
  • Cyclophosphamide
  • Dactinomycin
  • Doxorubicin
  • Hydroxyurea
  • Mechlorethamine
  • Melphalan
  • Mitoxantrone
  • Piroxicam
  • Procarbazine
  • Vinblastine
  • Vincristine

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