Home NDC 54771-8433-2 NDC 54771-8433-2 - Albon 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 54771-8433
Requested NDC 54771-8433-2
Package NDCs from labels 54771-8433-1, 54771-8433-2
Manufacturer Zoetis Inc.
Effective date 2019-11-07
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type ALBON ® Tablets Zoetis Inc. 2019-11-07 PRESCRIPTION ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 54771-8433-1 Albon 100 in 1 BOTTLE, PLASTIC TABLET 100 4 54771-8433-2 Albon 500 in 1 BOTTLE, PLASTIC TABLET 500 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 54771-8433 ALBON (SULFADIMETHOXINE) TABLET [ZOETIS INC.] 4 2 package rows 20191108_71a27a8a-038b-4b6d-8237-d6b58ddf9dc8.zip
DailyMed Socrata Ingredients# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.