FDA.reportPublic FDA data

NDC 17033-235-90 - Rederox

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
17033-235
Requested NDC
17033-235-90
Package NDCs from labels
17033-235-30, 17033-235-90
Manufacturer
Dechra Vet Products, LLC
Effective date
2026-02-12
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Rederox - Dechra Vet Products, LLCDechra Vet Products, LLC2026-02-12PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17033-235-30Rederox30 in 1 BOTTLETABLET, CHEWABLE303
17033-235-90Rederox90 in 1 BOTTLETABLET, CHEWABLE903

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17033-235REDEROX (DERACOXIB) TABLET, CHEWABLE [DECHRA VET PRODUCTS, LLC]22 package rows20230314_8ae1cdb9-8781-403c-a834-143ce47c3b8a.zip

Reported adverse events (FAERS/openFDA)#

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