Home NDC 58198-0630 NDC 58198-0630 - Optaflexx 45 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 58198-0630
Package NDCs from labels 58198-0630-9
Manufacturer Elanco US Inc.
Effective date 2026-01-16
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Optaflexx 45 - Elanco US Inc. Elanco US Inc. 2026-01-16 OTC TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58198-0630-9 Optaflexx 45 11.34 kg in 1 BAG POWDER 11.34 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58198-0630 OPTAFLEXX 45 (RACTOPAMINE HYDROCHLORIDE) POWDER [ELANCO US INC.] 5 1 package rows 20250114_48b0f54c-57ee-445b-9f53-817cfaba38ad.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.