Allergy Relief

Product NDC
68998-414
11-digit product format
689980414
Labeler code
68998
Product ID
68998-414_ad095cf5-0a18-4a1f-8881-b6b2cd4fa1f7
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
Marc Glassman, Inc.
Application
ANDA210722
Marketing category
ANDA
Marketing start
2020-05-01
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
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
68998-414-82Allergy Relief90 in 1 BOTTLETABLET904
68998-414-85Allergy Relief30 in 1 CARTONTABLET304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68998-414ALLERGY RELIEF (LORATADINE) TABLET [MARC GLASSMAN, INC.]4Current NDC, Legacy NDC, 2 package rows20230103_717ccb47-e13c-4464-b6e6-bea8f24d4663.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311372loratadine 10 MG 24HR Oral TabletPSN717ccb47-e13c-4464-b6e6-bea8f24d46634
311372loratadine 10 MG Oral TabletSCD717ccb47-e13c-4464-b6e6-bea8f24d46634
311372loratadine 10 MG 24 HR Oral TabletSY717ccb47-e13c-4464-b6e6-bea8f24d46634

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68998-414-826899804148290 TABLET in 1 BOTTLE (68998-414-82) 90 tablet2022-08-160000-00-00NoNoCurrent
68998-414-856899804148530 TABLET in 1 CARTON (68998-414-85) 30 tablet2020-05-010000-00-00NoNoCurrent