FDA.reportPublic FDA data

NDC 51927-5201 - OXIBENDAZOLE

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
51927-5201
Package NDCs from labels
51927-5201-0
Manufacturer
Professional Compounding Centers of America
Effective date
2023-01-12
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
OXIBENDAZOLE - Professional Compounding Centers of AmericaProfessional Compounding Centers of America2023-01-12BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51927-5201-0OXIBENDAZOLE1 kg in 1 BOTTLEPOWDER12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51927-5201OXIBENDAZOLE (OXIBENDAZOL) POWDER [PROFESSIONAL COMPOUNDING CENTERS OF AMERICA]21 package rows20241006_59011ebd-e5e1-494b-b59a-1d92b051f195.zip

Reported adverse events (FAERS/openFDA)#

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