Childrens Cetirizine Hydrochloride

Product NDC
62011-0093
11-digit product format
620110093
Labeler code
62011
Product ID
62011-0093_204a967a-0742-4b0a-9a24-e0ee7e44479b
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine hydrochloride
Dosage form
SOLUTION
Route
ORAL
Labeler
Health Mart
Application
ANDA201546
Marketing category
ANDA
Marketing start
2011-05-20
Marketing end
0000-00-00
Substance
CETIRIZINE HYDROCHLORIDE
Active strength
1 mg/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62011-0093-12021-09-08C16284748780-1ba0f9c33-4d90-a910-e053-dadaa90a0b850520a69c-87e0-4aba-8abd-4dbc0d6aff1e
62011-0093-12021-01-29C16284748780-1ba0f9c33-4d90-a910-e053-dadaa90a0b850520a69c-87e0-4aba-8abd-4dbc0d6aff1e

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62011-0093-1ML - Milliliter62011-00939ebbb345-19d6-4727-b157-7d2e5721842e12012-07-24