Home NDC 62991-3174 NDC 62991-3174 - Carprofen 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 62991-3174
Package NDCs from labels 62991-3174-1, 62991-3174-2
Manufacturer LETCO MEDICAL, LLC
Effective date 2026-04-07
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Carprofen - LETCO MEDICAL, LLC LETCO MEDICAL, LLC 2026-04-07 BULK INGREDIENT - ANIMAL DRUG
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 62991-3174-1 Carprofen 100 g in 1 JAR POWDER 100 5 62991-3174-2 Carprofen 500 g in 1 JAR POWDER 500 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62991-3174 CARPROFEN POWDER [LETCO MEDICAL, LLC] 3 2 package rows 20240719_89c93ca4-07cb-4ab5-bbe2-d079fedea25d.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.