Allergy Relief Non Drowsy

Product NDC
52904-430
11-digit product format
529040430
Labeler code
52904
Product ID
52904-430_467fa578-bb0b-48dd-b5e2-36e5e9829c96
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
Select Corporation
Application
ANDA077153
Marketing category
ANDA
Marketing start
2012-10-15
Marketing end
0000-00-00
Substance
LORATADINE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52904-430-012020-01-31C16284748780-19d75b9d0-6754-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52904-430-01Allergy Relief Non Drowsy1 in 1 PACKETTABLET11

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52904-430ALLERGY RELIEF NON DROWSY (LORATADINE) TABLET [SELECT CORPORATION]1Legacy NDC, 1 package rows20121107_f14b202e-56bd-4477-84c9-2d99ac38c111.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311372loratadine 10 MG 24HR Oral TabletPSNf14b202e-56bd-4477-84c9-2d99ac38c1111
311372loratadine 10 MG Oral TabletSCDf14b202e-56bd-4477-84c9-2d99ac38c1111
311372loratadine 10 MG 24 HR Oral TabletSYf14b202e-56bd-4477-84c9-2d99ac38c1111

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
52904-430-01529040430011 in 1 PACKETHistorical