Home NDC 58198-0039-3 NDC 58198-0039-3 - Veraflox 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 58198-0039
Requested NDC 58198-0039-3
Package NDCs from labels 58198-0039-3, 58198-0039-1
Manufacturer Elanco US Inc.
Effective date 2025-11-11
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Veraflox™ Elanco US Inc. 2025-11-11 PRESCRIPTION ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58198-0039-1 Veraflox 1 in 1 CARTON SUSPENSION 1 5 58198-0039-3 Veraflox 15 mL in 1 BOTTLE SUSPENSION 15 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58198-0039 VERAFLOX (PRADOFLOXACIN) SUSPENSION [ELANCO US INC.] 4 2 package rows 20221029_bc23bafe-9f6e-4253-84d1-3ff69b0a1f05.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.