FDA.reportPublic FDA data

Leader Childrens Allergy Relief

Product NDC
37205-570
11-digit product format
372050570
Labeler code
37205
Product ID
37205-570_5fe8e27a-ca58-48c1-ac51-468a24fa8b7e
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
SOLUTION
Route
ORAL
Labeler
Cardinal Health
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
37205-570-262025-04-16C16284748780-19d75b9d0-97f9-f424-e053-dadaa90a57cee411ab5b-9bce-463c-8ac3-8f204c6db1a1
37205-570-262020-01-31C16284748780-19d75b9d0-97f9-f424-e053-dadaa90a57cee411ab5b-9bce-463c-8ac3-8f204c6db1a1

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
37205-570-26ML - Milliliter37205-57074ca1b12-54ef-4f6d-b125-89848ea21dfe12014-07-02