FDA.reportPublic FDA data

NDC 86136-113-03 - OstiFen

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
86136-113
Requested NDC
86136-113-03
Package NDCs from labels
86136-113-65, 86136-113-36, 86136-113-03
Manufacturer
MWI/Vetone | FELIX PHARMACEUTICALS PRIVATE LIMITED
Effective date
2025-10-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
OstiFen - MWI/Vetone | FELIX PHARMACEUTICALS PRIVATE LIMITEDMWI/Vetone | FELIX PHARMACEUTICALS PRIVATE LIMITED2025-10-09Prescription Animal Drug Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86136-113-03OstiFen180 in 1 BOTTLETABLET1804
86136-113-36OstiFen60 in 1 BOTTLETABLET604
86136-113-65OstiFen30 in 1 BOTTLETABLET304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86136-113OSTIFEN (CARPROFEN) TABLET, CHEWABLE [MWI/VETONE]13 package rows20240316_caf911ae-6de4-4027-a0f2-1f843a8296e2.zip

Reported adverse events (FAERS/openFDA)#

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