FDA.reportPublic FDA data

NDC 71052-020-50 - Firocoxib

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
71052-020
Requested NDC
71052-020-50
Package NDCs from labels
71052-020-50
Manufacturer
DARMERICA, LLC
Effective date
2026-06-22
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Firocoxib - DARMERICA, LLCDARMERICA, LLC2026-06-22BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-020-50Firocoxib0.05 kg in 1 PACKAGEPOWDER0.054

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71052-020FIROCOXIB POWDER [DARMERICA, LLC]41 package rows20241222_ca9adba7-fab0-4652-accf-c092810a2286.zip

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.