Allergy Relief

Product NDC
50090-4266
11-digit product format
500904266
Labeler code
50090
Product ID
50090-4266_6aafc9be-454b-4b5c-b2c8-ca69b3f4dc00
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA075209
Marketing category
ANDA
Marketing start
2018-12-31
Marketing end
0000-00-00
Substance
LORATADINE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50090-4266-02023-01-30C16284748780-1f386c649-c8b4-0266-e053-dadaa90a7c1aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-4266-0Allergy ReliefNon drowsy30 in 1 BOTTLETABLET301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-4266ALLERGY RELIEF NON DROWSY (LORATADINE) TABLET [A-S MEDICATION SOLUTIONS]1Legacy NDC, 1 package rows20210303_c4b5ae13-da50-49d4-a76c-b2b3969596dd.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311372loratadine 10 MG 24HR Oral TabletPSNc4b5ae13-da50-49d4-a76c-b2b3969596dd1
311372loratadine 10 MG Oral TabletSCDc4b5ae13-da50-49d4-a76c-b2b3969596dd1
311372loratadine 10 MG 24 HR Oral TabletSYc4b5ae13-da50-49d4-a76c-b2b3969596dd1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-4266-05009042660030 TABLET in 1 BOTTLE (50090-4266-0) 30 tablet2019-04-170000-00-00NoNoCurrent