Cetirizine Hydrochloride

Product NDC
10544-670
11-digit product format
105440670
Labeler code
10544
Product ID
10544-670_14b4967f-6f33-4ade-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Blenheim Pharmacal, Inc.
Application
ANDA077829
Marketing category
ANDA
Marketing start
2009-10-01
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
10544-670-302020-01-31C16284748780-19d75b9d0-717a-f424-e053-dadaa90a57ceCetirizine Hydrochloride Tablets, 10 mg, Allergy

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10544-670-30Cetirizine Hydrochloride30 in 1 BOTTLETABLET302

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10544-670CETIRIZINE HYDROCHLORIDE TABLET [BLENHEIM PHARMACAL, INC.]2Legacy NDC, 1 package rows20150427_147e91e6-0840-05ee-e054-00144ff8d46c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1014678cetirizine HCl 10 MG Oral TabletPSN147e91e6-0840-05ee-e054-00144ff8d46c2
1014678cetirizine hydrochloride 10 MG Oral TabletSCD147e91e6-0840-05ee-e054-00144ff8d46c2
1014678cetirizine HCl 10 MG Oral TabletSY147e91e6-0840-05ee-e054-00144ff8d46c2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
10544-670-301054406703030 in 1 BOTTLEHistorical