Home NDC 54771-3520 NDC 54771-3520 - Solensia 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 54771-3520
Package NDCs from labels 54771-3520-1, 54771-3520-2
Manufacturer Zoetis Inc.
Effective date 2026-10-06
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Solensia® Zoetis Inc. 2026-10-06 PRESCRIPTION ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 54771-3520-1 Solensia 8 mL in 1 VIAL, GLASS SOLUTION 8 3 54771-3520-1 Solensia 2 in 1 CARTON SOLUTION 2 3 54771-3520-2 Solensia 20 mL in 1 VIAL, GLASS SOLUTION 20 3 54771-3520-2 Solensia 6 in 1 CARTON SOLUTION 6 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 54771-3520 SOLENSIA (FRUNEVETMAB) SOLUTION [ZOETIS INC.] 3 4 package rows 20221124_a73b79c4-3623-4b52-81ea-6180528a031e.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.