FDA product label FDA-initiated compliance action drug registration and listing inactivation 89600-1
LOINC Code
| LOINC code | 89600-1 | ||
|---|---|---|---|
| name | FDA product label FDA-initiated compliance action drug registration and listing inactivation | ||
| description | When a pharmaceutical company discontinues the marketing of a product, it is required to send the FDA an 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 The information is purged from the FDA database in order to eliminate outdated information. | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | FDA-initiated compliance action drug registration and listing inactivation | ||
| property | - | ||
| time | - | ||
| system | ^FDA product label | ||
| scale | Nar = Narrative: Text narrative, such as the description of a microscopic part of a surgical papule test. | ||
| method | |||
Additional Names | |||
| short name | FDA-init label compl act drug list inact | ||
Basic Attributes | |||
| class | DOC.REF | ||
| type | 2 Clinical | ||
| order vs. observation | Both | ||
Associated Observations | |||
LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations. | |||
History/Usage | |||
| first released | |||
| last updated | 2.65 | ||
| last change type | ADD - added | ||
Related Names | |||
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