Allegra Allergy

Product NDC
67751-173
11-digit product format
677510173
Labeler code
67751
Product ID
67751-173_3d30db81-64fd-681f-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
FEXOFENADINE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
Navajo Manufacturing Company Inc.
Application
NDA020872
Marketing category
NDA
Marketing start
2016-09-23
Marketing end
0000-00-00
Substance
FEXOFENADINE HYDROCHLORIDE
Active strength
180 mg/1
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
67751-173-012022-08-05C16284748780-19d75b9d0-166c-f424-e053-dadaa90a57ce84f13871-cd10-4554-8c72-39b83e198fd4
67751-173-012020-01-31C16284748780-19d75b9d0-166c-f424-e053-dadaa90a57ce84f13871-cd10-4554-8c72-39b83e198fd4