Home NDC 58198-0021-5 NDC 58198-0021-5 - Baytril 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 58198-0021
Requested NDC 58198-0021-5
Package NDCs from labels 58198-0021-3, 58198-0021-1, 58198-0021-4, 58198-0021-2, 58198-0021-5
Manufacturer Elanco US Inc.
Effective date 2026-05-07
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Elanco ™ Baytril TM 100 Elanco US Inc. 2026-05-07 PRESCRIPTION ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58198-0021-1 Baytril 1 in 1 CARTON INJECTION, SOLUTION 1 6 58198-0021-2 Baytril 1 in 1 CARTON INJECTION, SOLUTION 1 6 58198-0021-3 Baytril 100 mL in 1 BOTTLE INJECTION, SOLUTION 100 6 58198-0021-4 Baytril 250 mL in 1 BOTTLE INJECTION, SOLUTION 250 6 58198-0021-5 Baytril 500 mL in 1 BOTTLE INJECTION, SOLUTION 500 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58198-0021 BAYTRIL (ENROFLOXACIN) INJECTION, SOLUTION [ELANCO US INC.] 4 5 package rows 20250206_258967db-9587-4c19-b846-ac143dada99a.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.