Loratadine

Product NDC
58602-847
11-digit product format
586020847
Labeler code
58602
Product ID
58602-847_e24be27d-9c5e-4ff5-ae6d-96a6c1b6e710
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
Aurohealth LLC
Application
ANDA208314
Marketing category
ANDA
Marketing start
2020-05-16
Substance
LORATADINE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Loratadine
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LORATADINE10 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii7AJO3BO7QN
Rxcui311372

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58602-847-19Loratadine1 in 1 CARTONTABLET14
58602-847-19Loratadine90 in 1 BOTTLETABLET904
58602-847-29Loratadine150 in 1 BOTTLETABLET1504
58602-847-29Loratadine1 in 1 CARTONTABLET14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58602-847LORATADINE TABLET [AUROHEALTH LLC]4Current NDC, Legacy NDC, 4 package rows20220622_c6bfb54a-04d8-41c1-9fa9-5d4bae0a66d1.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311372loratadine 10 MG 24HR Oral TabletPSNc6bfb54a-04d8-41c1-9fa9-5d4bae0a66d14
311372loratadine 10 MG Oral TabletSCDc6bfb54a-04d8-41c1-9fa9-5d4bae0a66d14
311372loratadine 10 MG 24 HR Oral TabletSYc6bfb54a-04d8-41c1-9fa9-5d4bae0a66d14

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58602-847-19586020847191 BOTTLE in 1 CARTON (58602-847-19) / 90 TABLET in 1 BOTTLE1 bottle2020-05-160000-00-00NoNoCurrent
58602-847-29586020847291 BOTTLE in 1 CARTON (58602-847-29) / 150 TABLET in 1 BOTTLE1 bottle2020-08-130000-00-00NoNoCurrent