Home NDC 54771-1534-3 NDC 54771-1534-3 - Improvest 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 54771-1534
Requested NDC 54771-1534-3
Package NDCs from labels 54771-1534-3
Manufacturer Zoetis Inc.
Effective date 2020-05-05
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Improvest ® Zoetis Inc. 2020-05-05 PRESCRIPTION ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 54771-1534-3 Improvest 250 mL in 1 BOTTLE SOLUTION 250 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 54771-1534 IMPROVEST (GONADOTROPIN RELEASING FACTOR ANALOG-DIPHTHERIA TOXOID CONJUGATE) SOLUTION [ZOETIS INC.] 7 1 package rows 20200506_4262802d-a171-4439-baa1-dd88e5dded7b.zip
DailyMed Socrata Ingredients# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.