Loratadine

Product NDC
30142-066
11-digit product format
301420066
Labeler code
30142
Product ID
30142-066_2adde2b3-bab0-4d53-98d0-b64e0c2addda
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
KROGER COMPANY
Application
ANDA208314
Marketing category
ANDA
Marketing start
2021-03-15
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
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
30142-066-09Loratadine30 in 1 BOTTLETABLET304
30142-066-09Loratadine1 in 1 CARTONTABLET14
30142-066-54Loratadine70 in 1 BOTTLETABLET704
30142-066-54Loratadine1 in 1 CARTONTABLET14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30142-066LORATADINE TABLET [KROGER COMPANY]3Current NDC, Legacy NDC, 4 package rows20210409_b96831f5-5e75-c526-e053-2995a90a36ad.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311372loratadine 10 MG 24HR Oral TabletPSNb96831f5-5e75-c526-e053-2995a90a36ad4
311372loratadine 10 MG Oral TabletSCDb96831f5-5e75-c526-e053-2995a90a36ad4
311372loratadine 10 MG 24 HR Oral TabletSYb96831f5-5e75-c526-e053-2995a90a36ad4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
30142-066-09301420066091 BOTTLE in 1 CARTON (30142-066-09) / 30 TABLET in 1 BOTTLE1 bottle2021-03-150000-00-00NoNoCurrent
30142-066-54301420066541 BOTTLE in 1 CARTON (30142-066-54) / 70 TABLET in 1 BOTTLE1 bottle2021-03-150000-00-00NoNoCurrent