FDA.reportPublic FDA data

OXIBENDAZOLE

Manufacturer
PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC
Effective date
2021-12-21
Label type
BULK INGREDIENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:50:17

Label at a glance#

ProductOXIBENDAZOLE
Active ingredientOXIBENDAZOLE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

oxibendazolelabel.jpgPACKAGE LABEL IMAGEPACKAGE LABEL IMAGE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72969-117-10OXIBENDAZOLE1 g in 1 PACKAGEPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72969-117OXIBENDAZOLE POWDER [PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC]11 package rows20211223_905707f8-e748-4cd5-8ebe-75884c1e326f.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
72969-11772969-117-10

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
OXIBENDAZOLE022N12KJ0XACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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