FDA.reportPublic FDA data

NDC 86236-002-03 - DICLAZURIL

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
86236-002
Requested NDC
86236-002-03
Package NDCs from labels
86236-002-01, 86236-002-02, 86236-002-03, 86236-002-04, 86236-002-05
Manufacturer
Chongqing VPON Pharmaceutical Co., Ltd.
Effective date
2026-06-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
86236-(001-002)Chongqing VPON Pharmaceutical Co., Ltd.2026-06-24BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86236-002-01TOLTRAZURIL1 kg in 1 BAGPOWDER12
86236-002-02TOLTRAZURIL5 kg in 1 BAGPOWDER52
86236-002-03TOLTRAZURIL20 kg in 1 DRUMPOWDER202
86236-002-04TOLTRAZURIL25 kg in 1 DRUMPOWDER252
86236-002-05TOLTRAZURIL30 kg in 1 DRUMPOWDER302

Reported adverse events (FAERS/openFDA)#

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