Cetirizine

Product NDC
67046-680
11-digit product format
670460680
Labeler code
67046
Product ID
67046-680_6a707324-b32c-9741-e053-2a91aa0a2af2
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine
Dosage form
TABLET
Route
ORAL
Labeler
Contract Pharmacy Services-PA
Application
ANDA078336
Marketing category
ANDA
Marketing start
2018-02-14
Marketing end
0000-00-00
Substance
CETIRIZINE HYDROCHLORIDE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
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#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67046-680-30Cetirizine30 in 1 BLISTER PACKTABLET301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67046-680CETIRIZINE TABLET [CONTRACT PHARMACY SERVICES-PA]1Legacy NDC, 1 package rows20180422_6a707324-b32b-9741-e053-2a91aa0a2af2.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1014678cetirizine HCl 10 MG Oral TabletPSN6a707324-b32b-9741-e053-2a91aa0a2af21
1014678cetirizine hydrochloride 10 MG Oral TabletSCD6a707324-b32b-9741-e053-2a91aa0a2af21
1014678cetirizine HCl 10 MG Oral TabletSY6a707324-b32b-9741-e053-2a91aa0a2af21

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
67046-680-306704606803030 TABLET in 1 BLISTER PACK (67046-680-30) 30 tablet2018-02-140000-00-00NoNoCurrent