FDA.reportPublic FDA data

NDC 86228-001 - Ponazuril

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
86228-001
Package NDCs from labels
86228-001-01
Manufacturer
Shanghai Zhenhong Pharm Tech Co., Ltd.
Effective date
2025-04-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
86228-001Shanghai Zhenhong Pharm Tech Co., Ltd.2025-04-28BULK INGREDIENT - ANIMAL DRUG

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86228-001PONAZURIL POWDER [SHANGHAI ZHENHONG PHARM TECH CO., LTD.]1Unmatched20250507_cb9995ad-20b6-4b2d-82b3-6f4b02108524.zip

Reported adverse events (FAERS/openFDA)#

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