Childrens Loratadine

Product NDC
11822-0850
11-digit product format
118220850
Labeler code
11822
Product ID
11822-0850_b721e740-e60d-492e-86fd-f7b459b76d9c
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
SOLUTION
Route
ORAL
Labeler
Rite Aid Corporation
Application
ANDA076805
Marketing category
ANDA
Marketing start
2004-08-20
Marketing end
0000-00-00
Substance
LORATADINE
Active strength
5 mg/5mL
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-0850-82020-01-31C16284748780-19d75b9d0-0ee6-f424-e053-dadaa90a57ceChildren's Loratadine Syrup

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-0850-8Childrens Loratadine1 in 1 CARTONSOLUTION11
11822-0850-8Childrens Loratadine120 mL in 1 BOTTLESOLUTION1201

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-0850CHILDRENS LORATADINE (LORATADINE) SOLUTION [RITE AID CORPORATION]1Legacy NDC, 2 package rows20121113_73aaa515-1931-4bb1-b337-9e7be3fae159.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
692783loratadine 5 MG in 5 mL Oral SolutionPSN73aaa515-1931-4bb1-b337-9e7be3fae1591
692783loratadine 1 MG/ML Oral SolutionSCD73aaa515-1931-4bb1-b337-9e7be3fae1591
692783loratadine 5 MG per 5 ML Oral SolutionSY73aaa515-1931-4bb1-b337-9e7be3fae1591

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
11822-0850-8118220850081 in 1 CARTONHistorical