CVS Loratadine

Product NDC
51316-184
11-digit product format
513160184
Labeler code
51316
Product ID
51316-184_41c5ecce-51a2-733a-e063-6394a90a7327
Type
HUMAN OTC DRUG
Nonproprietary name
LORATADINE
Dosage form
TABLET
Route
ORAL
Labeler
CVS Pharmacy
Application
ANDA214684
Marketing category
ANDA
Marketing start
2025-10-22
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
CVS 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
51316-184-10CVS Loratadine365 in 1 BOTTLETABLET3653

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311372loratadine 10 MG 24HR Oral TabletPSN3d716988-da63-59e6-e063-6394a90a5b4b3
311372loratadine 10 MG Oral TabletSCD3d716988-da63-59e6-e063-6394a90a5b4b3
311372loratadine 10 MG 24 HR Oral TabletSY3d716988-da63-59e6-e063-6394a90a5b4b3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
51316-184-1051316018410365 TABLET in 1 BOTTLE (51316-184-10) 365 tablet2025-10-22NoNoCurrent