FDA.reportPublic FDA data

NDC 86101-042-90 - 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
86101-042
Requested NDC
86101-042-90
Package NDCs from labels
86101-042-30, 86101-042-90
Manufacturer
FELIX PHARMACEUTICALS PRIVATE LIMITED
Effective date
2026-07-10
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Carprofen - FELIX PHARMACEUTICALS PRIVATE LIMITEDFELIX PHARMACEUTICALS PRIVATE LIMITED2026-07-10Prescription Animal Drug Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86101-042-30Carprofen30 in 1 BOTTLETABLET303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86101-042CARPROFEN (CARPROFEN SOFT CHEWABLE) TABLET [FELIX PHARMACEUTICALS PRIVATE LIMITED]11 package rows20241215_1ea3e536-87d8-467c-a5c6-4af09f827212.zip

Reported adverse events (FAERS/openFDA)#

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