FDA.reportPublic FDA data

NDC 17030-250-60 - FLEXPROFEN

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
17030-250
Requested NDC
17030-250-60
Package NDCs from labels
17030-250-60, 17030-250-80
Manufacturer
Vetoquinol USA, Inc. | Felix Pharmaceuticals Private Limited
Effective date
2026-03-04
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
FLEXPROFEN - Vetoquinol USA, Inc. | Felix Pharmaceuticals Private LimitedVetoquinol USA, Inc. | Felix Pharmaceuticals Private Limited2026-03-04PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17030-250-60FLEXPROFEN60 in 1 BOTTLETABLET604
17030-250-80FLEXPROFEN180 in 1 BOTTLETABLET1804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17030-250FLEXPROFEN (CARPROFEN) TABLET [VETOQUINOL USA, INC.]32 package rows20250117_b65833ee-4415-4d3c-8ce1-d1827201548f.zip

Reported adverse events (FAERS/openFDA)#

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