What occurs if drugs do not meet compendium standards?

If drugs do not meet compendium standards, they may be considered adulterated. The term "adulterated" refers to products that are not manufactured, packaged, or labeled in accordance with the standards established by authoritative references such as the United States Pharmacopeia (USP) or other relevant compendium standards. These standards are in place to ensure that drugs are safe, effective, and of high quality.

If a drug fails to meet these standards, it raises concerns about its purity, strength, and overall quality, which can pose health risks to patients. Regulatory agencies, such as the FDA, may take action against such drugs, including removing them from the market or requiring recalls to protect public health. Understanding this concept is crucial for pharmacy technicians, as it emphasizes the importance of adhering to established standards for medication safety and reliability.