24 Hour Allergy

Product NDC
53187-189
11-digit product format
531870189
Labeler code
53187
Product ID
53187-189_30bdf288-c933-4867-9929-ef702c97ef9d
Type
HUMAN OTC DRUG
Nonproprietary name
Fexofenadine HCl
Dosage form
TABLET
Route
ORAL
Labeler
LIVE BETTER (The Great Atlantic & Pacific Tea Company)
Application
ANDA079112
Marketing category
ANDA
Marketing start
2013-03-20
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
53187-189-302024-04-10C16284748780-19d75b9d0-944b-f424-e053-dadaa90a57ce9c83780f-08c0-459e-98f7-147762eb4c21
53187-189-302020-01-31C16284748780-19d75b9d0-944b-f424-e053-dadaa90a57ce9c83780f-08c0-459e-98f7-147762eb4c21