Loratadine 10mg

Product NDC
21130-932
11-digit product format
211300932
Labeler code
21130
Product ID
21130-932_496f1885-3f87-6a87-e063-6394a90a65a5
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
BETTER LIVING BRANDS, LLC
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-04-18
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
Loratadine 10mg
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
21130-932-65Loratadine 10mg365 in 1 BOTTLETABLET3652
21130-932-65Loratadine 10mg1 in 1 CARTONTABLET12

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311372loratadine 10 MG 24HR Oral TabletPSN46d615dd-45d5-2dfc-e063-6394a90a5d422
311372loratadine 10 MG Oral TabletSCD46d615dd-45d5-2dfc-e063-6394a90a5d422
311372loratadine 10 MG 24 HR Oral TabletSY46d615dd-45d5-2dfc-e063-6394a90a5d422

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
21130-932-65211300932651 BOTTLE in 1 CARTON (21130-932-65) / 365 TABLET in 1 BOTTLE1 bottle2026-04-18NoNoHistorical