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Regulatory

Off-Label Use

Definition

The use of an FDA-approved drug for a purpose, population, or dosage other than what was approved. Many peptides prescribed by physicians are used off-label based on emerging research.

Related Terms in Regulatory

503A Pharmacy

A compounding pharmacy that prepares medications based on individual prescriptions. Subject to state board of pharmacy oversight.

503B Outsourcing Facility

A compounding facility registered with the FDA that can produce compounded medications in larger quantities without individual prescriptions, subject to FDA inspection.

Compounded Medication

A medication prepared by a licensed compounding pharmacy to meet an individual patient's specific needs. Subject to different regulations than manufactured drugs.

Research Use Only (RUO)

A regulatory designation indicating a product is intended solely for laboratory research and is not approved for human consumption or therapeutic use.

WADA (World Anti-Doping Agency)

The international organization responsible for promoting, coordinating, and monitoring anti-doping in sports. Many research peptides are on the WADA prohibited list.

FDA Category 2

Under FDA compounding rules, a substance placed on the Category 2 list is nominated for evaluation but has not yet been approved for use in compounding by 503A or 503B pharmacies. BPC-157 has been placed on this list.

FDA Category 1

Under FDA compounding rules, substances on the Category 1 list have been evaluated and approved as bulk drug substances eligible for compounding by 503A and 503B pharmacies.

Class II Recall

An FDA product recall classification indicating a situation where use of or exposure to the product may cause temporary or medically reversible adverse health consequences. All peptide-related FDA recalls to date have been Class II.

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