LOINC Code 99282-6: FDA product label FDA-initiated compliance action drug registration and listing inactivation - animal drug

What is this code?

LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component FDA-initiated compliance action drug registration and listing inactivation - animal drug. It is commonly used with the system or sample type ^FDA product label.

When is it used?

• Used in lab systems, EHRs, and clinical data exchange.
• May identify a test, observation, survey item, or clinical document request rather than a diagnosis.
• Status: ACTIVE
• Order vs observation: Both

What it does not mean

• The code identifies the observation or test, not the actual result.

Key facts

• FDA product label FDA-initiated compliance action drug registration and listing inactivation - animal drug
• FDA-initiated compliance action drug registration and listing inactivation - animal drug
• When a pharmaceutical company discontinues the marketing of a product, it is required to send the FDA an Structured Product Labeling (SPL) file to indicate their intention to stop selling the drug. If no SPL file is received by a certain time, the FDA inactivates the drug listing. The information is purged from the FDA database in order to eliminate outdated information.
• DOCUMENT.REF; Drugs; FDA compl action drug and list inact; FDA drug+list inactive - animal drug; FDA label; Narrative; Report

Where you may see this code

You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges.

Common synonyms

Frequently asked questions