Home NDC 46016-1470-0 NDC 46016-1470-0 - Maropitant 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 46016-1470
Requested NDC 46016-1470-0
Package NDCs from labels 46016-1470-0
Manufacturer PROCOS SpA
Effective date 2022-03-22
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Maropitant - PROCOS SpA PROCOS SpA 2022-03-22 BULK INGREDIENT - ANIMAL DRUG
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 46016-1470-0 Maropitant 50 kg in 1 CONTAINER POWDER 50 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 46016-1470 MAROPITANT POWDER [PROCOS SPA] 4 1 package rows 20220323_14091980-47cc-41cb-a75b-0671efd0d22d.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.