99282-6
ClinicalFDA product label FDA-initiated compliance action drug registration and listing inactivation - animal drug
Definition
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 The information is purged from the FDA database in order to eliminate outdated information.
LOINC 6-Axis Classification
Component
FDA-initiated compliance action drug registration and listing inactivation - animal drug
Property
-
Time Aspect
-
System
^FDA product label
Scale Type
Nar
Method Type
N/A
Details
Class
DOC.REF
Order/Observation
Both
Short Name
FDA animal drug+list inactivation
Related Names
Frequently Asked Questions
What is LOINC code 99282-6?
LOINC code 99282-6 identifies "FDA product label 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 The information is purged from the FDA database in order to eliminate outdated information.
What does 99282-6 measure?
This code measures FDA-initiated compliance action drug registration and listing inactivation - animal drug in ^FDA product label. It belongs to the DOC.REF class in the LOINC classification.
What is LOINC?
LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.