FDA.reportPublic FDA data

FEBANTEL

Manufacturer
F.I.S. Fabbrica Italiana Sintetici S.P.A.
Effective date
2024-11-22
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
4
Source
full-release
Hydrated at
2026-06-01 02:51:17

Label at a glance#

ProductFEBANTEL
Active ingredientFEBANTEL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Febantel_U31Febantel_U31

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52133-0047-0FEBANTEL50 kg in 1 DRUMPOWDER504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52133-0047FEBANTEL POWDER [F.I.S. FABBRICA ITALIANA SINTETICI S.P.A.]41 package rows20241127_ce164a56-ddfb-6098-e053-2a95a90add22.zip

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
52133-004752133-0047-0

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
FEBANTELS75C401OS1ACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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