FDA.reportPublic FDA data

NDC 51072-116-01 - EquiCoxib

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
51072-116
Requested NDC
51072-116-01
Package NDCs from labels
51072-116-00, 51072-116-01
Manufacturer
Aurora Pharmaceutical, Inc.
Effective date
2025-12-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
EquiCoxib™ (firocoxib) Oral Solution for HorsesAurora Pharmaceutical, Inc.2025-12-11PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51072-116-00EquiCoxib1 in 1 CARTONSOLUTION13
51072-116-00EquiCoxib90 mL in 1 BOTTLESOLUTION903
51072-116-01EquiCoxib400 mL in 1 BOTTLESOLUTION4003
51072-116-01EquiCoxib1 in 1 CARTONSOLUTION13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51072-116EQUICOXIB (FIROCOXIB) SOLUTION [AURORA PHARMACEUTICAL, INC.]24 package rows20241010_f1456f2e-0aae-4f11-b3d7-da81b8eb33cb.zip

Reported adverse events (FAERS/openFDA)#

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