Home NDC 58198-4886 NDC 58198-4886 - Onsior 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 58198-4886
Package NDCs from labels 58198-4886-1
Manufacturer Elanco US Inc.
Effective date 2026-05-19
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type onsior™ (robenacoxib) Elanco US Inc. 2026-05-19 PRESCRIPTION ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58198-4886-1 Onsior 1 in 1 CARTON INJECTION 1 5 58198-4886-1 Onsior 20 mL in 1 VIAL INJECTION 20 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58198-4886 ONSIOR (ROBENACOXIB) INJECTION [ELANCO US INC.] 3 2 package rows 20201126_f4f307a0-88b5-4740-b198-35edef954bf1.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.