FDA.reportPublic FDA data

NDC 73377-078 - Flunixin Meglumine

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
73377-078
Package NDCs from labels
73377-078-01, 73377-078-02, 73377-078-03
Manufacturer
AX Pharmaceutical Corp
Effective date
2023-12-13
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Flunixin Meglumine - AX Pharmaceutical CorpAX Pharmaceutical Corp2023-12-13BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73377-078-01Flunixin Meglumine0.5 kg in 1 JARPOWDER0.52
73377-078-02Flunixin Meglumine25 kg in 1 DRUMPOWDER252
73377-078-03Flunixin Meglumine20 kg in 1 DRUMPOWDER202

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73377-078FLUNIXIN MEGLUMINE POWDER [AX PHARMACEUTICAL CORP]23 package rows20231214_b4a6aaa9-bcdd-44d9-b84d-92c99a51cd1d.zip

Reported adverse events (FAERS/openFDA)#

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