NDC 58198-5567 - Experior 50

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
58198-5567
Package NDCs from labels
58198-5567-1
Manufacturer
Elanco US Inc.
Effective date
2024-06-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Elancoâ„¢Elanco US Inc.2024-06-05OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58198-5567-1Experior 5010 kg in 1 BAGGRANULE103

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58198-5567EXPERIOR 50 (LUBABEGRON) GRANULE [ELANCO US INC.]31 package rows20240615_631a7444-8652-4bbd-907e-87f6b32cbac7.zip

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.