FDA.reportPublic FDA data

Flunixin Meglumine

Manufacturer
AMERICAN PHARMACEUTICAL INGREDIENTS LLC
Effective date
2014-04-25
Label type
BULK INGREDIENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:47:56

Label at a glance#

ProductFlunixin Meglumine
Active ingredientFlunixin Meglumine
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58597-8272-4Flunixin Meglumine25 g in 1 BOTTLEPOWDER251
58597-8272-6Flunixin Meglumine100 g in 1 BOTTLEPOWDER1001
58597-8272-8Flunixin Meglumine1000 g in 1 BOTTLEPOWDER10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58597-8272FLUNIXIN MEGLUMINE POWDER [AMERICAN PHARMACEUTICAL INGREDIENTS LLC]13 package rows20140428_c4a5496b-ca45-4a9f-b84f-625d08eb1a2c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Flunixin MeglumineACTIVE INGREDIENT8Y3JK0JW3U1
Flunixin MeglumineACTIVE MOIETY8Y3JK0JW3U1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58597-827258597-8272-4, 58597-8272-6, 58597-8272-8

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
Flunixin Meglumine8Y3JK0JW3UACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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