FDA.reportPublic FDA data

NDC 86225-001 - Atipamezole Base

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
86225-001
Package NDCs from labels
86225-001-01, 86225-001-02, 86225-001-03
Manufacturer
Nanjing Zhongdali 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
86225-001Nanjing Zhongdali Pharm Tech Co., Ltd.2025-04-28BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86225-001-01Atipamezole Base25 g in 1 BAGPOWDER252
86225-001-02Atipamezole Base50 g in 1 BAGPOWDER502
86225-001-03Atipamezole Base1000 g in 1 BAGPOWDER10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86225-001ATIPAMEZOLE BASE POWDER [NANJING ZHONGDALI PHARM TECH CO., LTD.]13 package rows20250507_cbcae45d-37bb-4f56-bbd5-45e77e11192c.zip

Reported adverse events (FAERS/openFDA)#

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