Home NDC 54771-1128-0 NDC 54771-1128-0 - Robenz 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 54771-1128
Requested NDC 54771-1128-0
Package NDCs from labels 54771-1128-0
Manufacturer Zoetis Inc. | Zoetis LLC
Effective date 2020-04-08
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Robenz - Zoetis Inc. | Zoetis LLC Zoetis Inc. | Zoetis LLC 2020-04-08 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 54771-1128-0 Robenz 22.68 kg in 1 BAG POWDER 22.68 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 54771-1128 ROBENZ (ROBENIDINE HYDROCHLORIDE) POWDER [ZOETIS INC.] 2 1 package rows 20200418_f86501dd-61c8-451b-ad5e-562e349fbd37.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.