What does this LOINC code represent?

This LOINC code identifies a lab observation, measurement, question, or clinical concept in a standardized format.

Is this enough to understand my test result?

No. The code identifies the test or observation, but the interpretation depends on the actual result, reference range, and clinical context.

LOINCActiveObservation

LOINC Code 71743-9: FDA product label Generic drug facility identification submission

Name: LOINC Code 71743-9: FDA product label Generic drug facility identification submission
Creator: HealthAssure Clinical Team
Published: 2026-05-21T08:59:50.624Z

71743-9 is a LOINC code used to identify FDA product label Generic drug facility identification submission in laboratory and clinical observation data. You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges. LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Generic drug facility identification submission. It is commonly used with the system or sample type ^FDA product label.

Reviewed by HealthAssure Clinical TeamUpdated 21 May 2026

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 Generic drug facility identification submission. 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: Observation

What it does not mean

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

Key facts

FDA product label Generic drug facility identification submission
Generic drug facility identification submission
DOCUMENT.REF; Drugs; FDA label; Generic facility ID sub; 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

FDA product label Generic drug facility identification submissionFDA label Generic facility ID subGeneric drug facility identification submissionDOC.REF-^FDA product labelNar

Frequently asked questions

Code details

Code71743-9

SystemLOINC

Display nameFDA product label Generic drug facility identification submission

DescriptionGeneric drug facility identification submission

Short nameFDA label Generic facility ID sub

ComponentGeneric drug facility identification submission

Property-

Timing-

System (specimen)^FDA product label

ScaleNar

ClassDOC.REF

StatusACTIVE

Order/ObservationObservation

Flags

BillableNo

Valid clinical useNo

Source

SourceLOINC

Version2.82

Releasemain

First released2.40

Last changed2.67

Part names

Generic drug facility identification submission-^FDA product labelNar

About this content

This page is prepared by HealthAssure's clinical team using official coding standards from LOINC. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.