Home NDC 54771-8729 NDC 54771-8729 - Triamulox 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 54771-8729
Package NDCs from labels 54771-8729-0, 54771-8729-1
Manufacturer Zoetis Inc.
Effective date 2020-10-12
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type TriamuloxLiquid Concentrate Zoetis Inc. 2020-10-12 OTC ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 54771-8729-0 Triamulox 946 mL in 1 BOTTLE LIQUID 946 6 54771-8729-1 Triamulox 4730 mL in 1 BOTTLE LIQUID 4730 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 54771-8729 TRIAMULOX (TIAMULIN HYDROGEN FUMARATE) LIQUID [ZOETIS INC.] 6 2 package rows 20201013_d6fe4eee-f207-462f-9663-b7bce1017ca0.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.