Loratadine ODT

Product NDC
21130-221
11-digit product format
211300221
Labeler code
21130
Product ID
21130-221_57487b79-812f-4626-a068-be397bb1f7fd
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Labeler
Better Living Brands, LLC
Application
ANDA208477
Marketing category
ANDA
Marketing start
2023-09-20
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 ODT
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LORATADINE10 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii7AJO3BO7QN
Rxcui311373

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21130-221-84Loratadine ODT3 in 1 CARTONTABLET, ORALLY DISINTEGRATING32
21130-221-84Loratadine ODT10 in 1 BLISTER PACKTABLET, ORALLY DISINTEGRATING102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21130-221LORATADINE ODT (LORATADINE) TABLET, ORALLY DISINTEGRATING [BETTER LIVING BRANDS, LLC]2Current NDC, 2 package rows20230925_fad93257-bfcf-5e04-e053-6394a90a10a6.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311373loratadine 10 MG 24HR Disintegrating Oral TabletPSNfad93257-bfcf-5e04-e053-6394a90a10a62
311373loratadine 10 MG Disintegrating Oral TabletSCDfad93257-bfcf-5e04-e053-6394a90a10a62

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
21130-221-84211300221843 BLISTER PACK in 1 CARTON (21130-221-84) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK3 blister pack2023-09-20NoNoCurrent