All Day Allergy

Product NDC
41520-129
11-digit product format
415200129
Labeler code
41520
Product ID
41520-129_935b245a-3cfc-4640-9c1a-0466971776d7
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine HCl
Dosage form
TABLET
Route
ORAL
Labeler
Care One (American Sales Company)
Application
ANDA078780
Marketing category
ANDA
Marketing start
2010-09-07
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
41520-129-142025-02-27C16284748780-19d75b9d0-b65f-f424-e053-dadaa90a57cec7571a80-9613-45f7-a1a9-fde4943f487e
41520-129-142020-01-31C16284748780-19d75b9d0-b65f-f424-e053-dadaa90a57cec7571a80-9613-45f7-a1a9-fde4943f487e