All Day Allergy

Product NDC
53187-220
11-digit product format
531870220
Labeler code
53187
Product ID
53187-220_521a2311-5b96-443e-aef1-b2f406eafb6b
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine HCl
Dosage form
TABLET
Route
ORAL
Labeler
LIVE BETTER (The Great Atlantic & Pacific Tea Company)
Application
ANDA078427
Marketing category
ANDA
Marketing start
2013-06-07
Marketing end
0000-00-00
Substance
CETIRIZINE HYDROCHLORIDE
Active strength
10 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
53187-220-302024-04-10C16284748780-19d75b9d0-0f16-f424-e053-dadaa90a57ce9807bbac-84d5-4edd-ba0c-c294079d6157
53187-220-302020-01-31C16284748780-19d75b9d0-0f16-f424-e053-dadaa90a57ce9807bbac-84d5-4edd-ba0c-c294079d6157