All Day Allergy Relief

Product NDC
79903-437
11-digit product format
799030437
Labeler code
79903
Product ID
79903-437_25fa124f-d265-4c12-9703-6e2cfe340418
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
WALMART INC. (see also Equate)
Application
ANDA075209
Marketing category
ANDA
Marketing start
2026-04-01
Substance
LORATADINE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
All Day Allergy Relief
Listing expiration
2027-12-31

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
79903-437-12All Day Allergy Relief120 in 1 BOTTLE, PLASTICTABLET1203
79903-437-36All Day Allergy Relief365 in 1 BOTTLE, PLASTICTABLET3653

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311372loratadine 10 MG 24HR Oral TabletPSN80958503-400c-422a-a641-e1a3d5a9a6a83
311372loratadine 10 MG Oral TabletSCD80958503-400c-422a-a641-e1a3d5a9a6a83
311372loratadine 10 MG 24 HR Oral TabletSY80958503-400c-422a-a641-e1a3d5a9a6a83

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
79903-437-1279903043712120 TABLET in 1 BOTTLE, PLASTIC (79903-437-12) 120 tablet2026-04-01NoNoHistorical
79903-437-3679903043736365 TABLET in 1 BOTTLE, PLASTIC (79903-437-36) 365 tablet2026-04-01NoNoHistorical