Home NDC 54771-1457-1 NDC 54771-1457-1 - Bovatec 150FP 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 54771-1457
Requested NDC 54771-1457-1
Package NDCs from labels 54771-1457-1
Manufacturer Zoetis Inc.
Effective date 2020-06-10
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Bovatec ® 150 FP Zoetis Inc. 2020-06-10 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 54771-1457-1 Bovatec 150FP 22.68 kg in 1 BAG POWDER 22.68 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 54771-1457 BOVATEC 150FP (LASALOCID SODIUM) POWDER [ZOETIS INC.] 4 1 package rows 20200612_dd4b2577-e679-4949-92ce-d40082abb0e3.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.