Childrens allergy relief

Product NDC
41163-426
11-digit product format
411630426
Labeler code
41163
Product ID
41163-426_b3ac6c07-a06e-43eb-83ed-379a8a0ce200
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
SOLUTION
Route
ORAL
Labeler
Supervalu Inc
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
41163-426-852025-11-20C16284748780-19d75b9d0-bf32-f424-e053-dadaa90a57ce4669af7a-200c-4931-bfee-796ba4195944
41163-426-852020-01-31C16284748780-19d75b9d0-bf32-f424-e053-dadaa90a57ce4669af7a-200c-4931-bfee-796ba4195944

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41163-426CHILDRENS ALLERGY RELIEF (LORATADINE) SOLUTION [SUPERVALU INC]1Legacy NDC20121025_4669af7a-200c-4931-bfee-796ba4195944.zip