24-Hour All Day Allergy

Product NDC
62011-0052
11-digit product format
620110052
Labeler code
62011
Product ID
62011-0052_9af9e102-bddf-48ba-a636-773f6c665305
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine HCl
Dosage form
TABLET
Route
ORAL
Labeler
McKesson
Application
ANDA078780
Marketing category
ANDA
Marketing start
2012-04-27
Marketing end
0000-00-00
Substance
CETIRIZINE HYDROCHLORIDE
Active strength
10 mg/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62011-0052-1EA - Each62011-00522f45597a-6614-46aa-94a1-4d6c3496ca3012012-07-24
62011-0052-2EA - Each62011-0052d31f9dc2-0a3d-4bef-bb4c-f37b409e3c4712012-07-24