Why purchase pre-packaged medications?
State and Federal regulations state that dispensing is allowed through the physician practice only if the medications are properly packaged and labeled. Products must comply to federally mandated current Good Manufacturing Practices (GMP’s) as noted in Title 21 of Code of Federal Regulations. Noncompliance with these laws could render the medication as “adulterated” and or “misbranded”. It is a federal crime to dispense an adulterated or misbranded medication to a patient.
