Home NDC 13985-709 NDC 13985-709 - Enrosite 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 13985-709
Package NDCs from labels 13985-709-20, 13985-709-50
Manufacturer MWI/VetOne | Norbrook Laboratories Limited
Effective date 2026-05-13
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 13985-709-20 Enrosite 20 mL in 1 VIAL, GLASS INJECTION, SOLUTION 20 5 13985-709-20 Enrosite 1 in 1 CARTON INJECTION, SOLUTION 1 5 13985-709-50 Enrosite 1 in 1 CARTON INJECTION, SOLUTION 1 5 13985-709-50 Enrosite 50 mL in 1 VIAL, GLASS INJECTION, SOLUTION 50 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 13985-709 ENROSITE (ENROFLOXACIN) INJECTION, SOLUTION [MWI/VETONE] 4 4 package rows 20230910_9495fb96-0c56-409d-a2e9-12fed06e85a2.zip
DailyMed Socrata Ingredients#