Home NDC 54771-5278 NDC 54771-5278 - Spectramast DC 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 54771-5278
Package NDCs from labels 54771-5278-1, 54771-5278-2
Manufacturer Zoetis Inc.
Effective date 2025-03-26
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type SPECTRAMAST ® DC Zoetis Inc. 2025-03-26 PRESCRIPTION ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 54771-5278-1 SpectramastDC 12 in 1 CARTON SUSPENSION 12 5 54771-5278-1 SpectramastDC 10 mL in 1 SYRINGE SUSPENSION 10 5 54771-5278-2 SpectramastDC 144 in 1 PAIL SUSPENSION 144 5 54771-5278-2 SpectramastDC 10 mL in 1 SYRINGE SUSPENSION 10 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 54771-5278 SPECTRAMAST DC (CEFTIOFUR HYDROCHLORIDE) SUSPENSION [ZOETIS INC.] 5 4 package rows 20250402_eea5a063-8583-4f9b-8377-aa4c7e9fd302.zip
DailyMed Socrata Ingredients# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.