Flunixin Meglumine

Manufacturer
LETCO MEDICAL, LLC
Effective date
2026-09-23
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
19
Source
daily-update
Hydrated at
2026-09-25 02:02:07

Label at a glance#

ProductFlunixin Meglumine
Active ingredientFLUNIXIN MEGLUMINE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Flunixin Meglumine USP 100G
Flunixin Meglumine USP 100G

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeData Matrix(01)00362991160423(10)000000000(17)280817GTIN-14: 00362991160423
GTIN-12: 362991160423
UPC-A: 362991160423
EAN-13: 0362991160423
GTIN storage (14 digits): 00362991160423
flunixin-meglumine-1.jpg

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62991-1604-1GM - Gram62991-16046b2c2075-8279-403a-b54e-de276a45a01a12014-10-03
62991-1604-2GM - Gram62991-160442b6799c-0aa9-4a1a-8924-eadb52ed473b12014-10-03
62991-1604-4GM - Gram62991-1604c0a50789-d538-49b9-a1d9-fc7393c841f712014-10-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
FLUNIXIN MEGLUMINEACTIVE INGREDIENT8Y3JK0JW3U8
FLUNIXINACTIVE MOIETY356IB1O4008

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62991-160462991-1604-2, 62991-1604-4, 62991-1604-5

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
182025-06-27monthly-update2026-07-17 21:37:26
172025-06-27full-release2026-06-01 02:51:48

Reported adverse events (FAERS/openFDA)#

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