Which agency requires manufacturers to imprint special identification codes on orally available solid dosage forms?

The agency responsible for requiring manufacturers to imprint special identification codes on orally available solid dosage forms is the FDA (Food and Drug Administration). The FDA mandates that certain solid dosage forms, such as tablets and capsules, bear identifying characteristics that enhance patient safety and enable easier identification of medications. This requirement helps prevent medication errors and enhances traceability in the event of a recall or adverse reaction.

The Code of Federal Regulations (CFR) provides a comprehensive framework of regulations, but it is the FDA that specifically enforces the requirement for identification codes on solid dosage forms. Understanding the role of the FDA in drug regulation is crucial for navigating pharmaceutical jurisprudence.