Home NDC 54771-1685-3 NDC 54771-1685-3 - Valcor 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 54771-1685
Requested NDC 54771-1685-3
Package NDCs from labels 54771-1685-1, 54771-1685-2, 54771-1685-3
Manufacturer Zoetis Inc.
Effective date 2025-08-13
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type VALCOR ® Zoetis Inc. 2025-08-13 PRESCRIPTION ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 54771-1685-1 Valcor 100 mL in 1 VIAL, GLASS INJECTION, SOLUTION 100 4 54771-1685-2 Valcor 250 mL in 1 VIAL, GLASS INJECTION, SOLUTION 250 4 54771-1685-3 Valcor 500 mL in 1 VIAL, GLASS INJECTION, SOLUTION 500 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 54771-1685 VALCOR (DORAMECTIN AND LEVAMISOLE) INJECTION, SOLUTION [ZOETIS INC.] 3 3 package rows 20250326_ceeeee6b-011a-4d2f-a90a-d2958a9f12f9.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.