Cetirizine Hydrochloride

Product NDC
66336-336
11-digit product format
663360336
Labeler code
66336
Product ID
66336-336_64486ca9-85d5-40d1-9a5b-01d52521ed7b
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Dispensing Solutions, Inc.
Application
ANDA077946
Marketing category
ANDA
Marketing start
2007-12-27
Marketing end
0000-00-00
Substance
CETIRIZINE HYDROCHLORIDE
Active strength
10 mg/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c505bb17-4ff9-45f9-ac2d-bb9c8c9d35beProduct name120200304
a255659f-db40-429d-8c07-5f173f330d9cProduct name120190402

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66336-336-142019-11-13C16284748780-197449f38-c5e4-f6ea-e053-dbdaa90aa703Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66336-336-14Cetirizine Hydrochloride14 in 1 BOTTLETABLET143

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66336-336CETIRIZINE HYDROCHLORIDE TABLET [DISPENSING SOLUTIONS, INC.]3Legacy NDC, 1 package rows20120928_dd37b7c4-00d6-4a69-8213-713db5725e7c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1014678cetirizine HCl 10 MG Oral TabletPSNdd37b7c4-00d6-4a69-8213-713db5725e7c3
1014678cetirizine hydrochloride 10 MG Oral TabletSCDdd37b7c4-00d6-4a69-8213-713db5725e7c3
1014678cetirizine HCl 10 MG Oral TabletSYdd37b7c4-00d6-4a69-8213-713db5725e7c3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
66336-336-146633603361414 in 1 BOTTLEHistorical