Home NDC 58198-0020 NDC 58198-0020 - 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 58198-0020
Package NDCs from labels 58198-0020-1, 58198-0020-2
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 Baytril - Elanco US Inc. 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 58198-0020-1 Baytril 20 mL in 1 BOTTLE INJECTION, SOLUTION 20 8 58198-0020-2 Baytril 1 in 1 CARTON INJECTION, SOLUTION 1 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58198-0020 BAYTRIL (ENROFLOXACIN) INJECTION, SOLUTION [ELANCO US INC.] 6 2 package rows 20250206_a1ada9f6-24e2-4287-8b83-00e2b68666e5.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.