Home NDC 54771-6291-1 NDC 54771-6291-1 - Dormosedan 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 54771-6291
Requested NDC 54771-6291-1
Package NDCs from labels 54771-6291-1
Manufacturer Zoetis Inc.
Effective date 2022-05-16
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type DORMOSEDAN® GEL Zoetis Inc. 2022-05-16 PRESCRIPTION ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 54771-6291-1 Dormosedan 1 in 1 CARTON GEL 1 3 54771-6291-1 Dormosedan 3 mL in 1 SYRINGE, PLASTIC GEL 3 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 54771-6291 DORMOSEDAN (DETOMIDINE HYDROCHLORIDE) GEL [ZOETIS INC.] 3 2 package rows 20220517_bc3e8186-ba9e-4d74-88cf-cccb2f43fe2f.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.