Loratadine Allergy Relief

Product NDC
67091-246
11-digit product format
670910246
Labeler code
67091
Product ID
67091-246_53fce6fc-65d0-4fac-b3e0-b54865d8b158
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
WinCo Foods, LLC
Application
ANDA076134
Marketing category
ANDA
Marketing start
2003-08-28
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 Allergy Relief
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
67091-246-30Loratadine Allergy Relief1 in 1 BLISTER PACKTABLET12
67091-246-30Loratadine Allergy Relief30 in 1 CARTONTABLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67091-246LORATADINE ALLERGY RELIEF (LORATADINE) TABLET [WINCO FOODS, LLC]2Current NDC, Legacy NDC, 2 package rows20180831_506a60e8-7fec-4bb0-babc-204058ae120f.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311372loratadine 10 MG 24HR Oral TabletPSN506a60e8-7fec-4bb0-babc-204058ae120f2
311372loratadine 10 MG Oral TabletSCD506a60e8-7fec-4bb0-babc-204058ae120f2
311372loratadine 10 MG 24 HR Oral TabletSY506a60e8-7fec-4bb0-babc-204058ae120f2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
67091-246-306709102463030 BLISTER PACK in 1 CARTON (67091-246-30) / 1 TABLET in 1 BLISTER PACK30 blister pack2015-01-080000-00-00NoNoCurrent