Home NDC 54771-5279-1 NDC 54771-5279-1 - Spectramast LC 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 54771-5279
Requested NDC 54771-5279-1
Package NDCs from labels 54771-5279-1, 54771-5279-2
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 ® LC 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 54771-5279-1 SpectramastLC 10 mL in 1 SYRINGE SUSPENSION 10 8 54771-5279-1 SpectramastLC 12 in 1 CARTON SUSPENSION 12 8 54771-5279-2 SpectramastLC 144 in 1 PAIL SUSPENSION 144 8 54771-5279-2 SpectramastLC 10 mL in 1 SYRINGE SUSPENSION 10 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 54771-5279 SPECTRAMAST LC (CEFTIOFUR HYDROCHLORIDE) SUSPENSION [ZOETIS INC.] 8 4 package rows 20250402_35017960-b3c3-4e05-803c-e4a8b7009d83.zip
DailyMed Socrata Ingredients# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.