Home NDC 58198-5567-1 NDC 58198-5567-1 - 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
Requested NDC 58198-5567-1
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 Label Manufacturer Effective date Type Elanco™ Elanco US Inc. 2024-06-05 OTC ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58198-5567-1 Experior 50 10 kg in 1 BAG GRANULE 10 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58198-5567 EXPERIOR 50 (LUBABEGRON) GRANULE [ELANCO US INC.] 3 1 package rows 20240615_631a7444-8652-4bbd-907e-87f6b32cbac7.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.