
Compounding has been an essential part of pharmacy practice for centuries. Many regulatory bodies are aware of the practice of compounding and have set rules with which pharmacies must be compliant. The Food and Drug Administration allows products to be compounded as long as licensed practitioners have written a prescription for a specific patient to be filled at a licensed pharmacy. In addition, many state boards of pharmacy require additional regulations to be followed. Depending on the category of products made by your pharmacy, their compounding lab and procedures must be either USP 795 (for nonsterile) and/or USP 797 (for sterile) compliant.
Reviewed: July 16, 2021
Updated: July 28, 2021
Reviewed by: Stuart Berlin, PharmD

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