FDA.reportPublic FDA data

Ponazuril

Manufacturer
Willow Birch Pharma, Inc. | Alivira Animal Health Limited
Effective date
2022-09-20
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
1
Source
full-release
Hydrated at
2026-06-01 02:50:32

Label at a glance#

ProductPonazuril
Active ingredientPONAZURIL
Label structure1 sections

Label contents#

Full prescribing information#

Ponazuril

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PonazurilPonazuril

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10695-138-10Ponazuril1 kg in 1 PACKAGEPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10695-138PONAZURIL POWDER [WILLOW BIRCH PHARMA, INC.]11 package rows20220921_9f3700af-ab88-4fbf-8b77-0f1484aecd38.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
10695-13810695-138-10
86055-0009

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
PONAZURILJPW84AS66UACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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