FDA.reportPublic FDA data

NDC 13985-748 - 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
13985-748
Package NDCs from labels
13985-748-20, 13985-748-50
Manufacturer
MWI/VetOne | Norbrook Laboratories Limited
Effective date
2023-09-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
OstiFen - MWI/VetOne | Norbrook Laboratories LimitedMWI/VetOne | Norbrook Laboratories Limited2023-09-08PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
13985-748-20OstiFen20 mL in 1 VIAL, GLASSINJECTION, SOLUTION204
13985-748-20OstiFen1 in 1 CARTONINJECTION, SOLUTION14
13985-748-50OstiFen50 mL in 1 VIAL, GLASSINJECTION, SOLUTION504
13985-748-50OstiFen1 in 1 CARTONINJECTION, SOLUTION14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
13985-748OSTIFEN (CARPROFEN) INJECTION, SOLUTION [MWI/VETONE]44 package rows20230913_323a2312-192e-4747-841e-cb387d69e8bc.zip

Reported adverse events (FAERS/openFDA)#

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