NDC 73309-364 - Detomidine HCl

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
73309-364
Package NDCs from labels
73309-364-01
Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2022-03-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Detomidine HCl - BLUEBAY SHANDONG CO.,LTDBLUEBAY SHANDONG CO.,LTD2022-03-11BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-364-01Detomidine HCl50 g in 1 JARPOWDER501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-364DETOMIDINE HCL POWDER [BLUEBAY SHANDONG CO.,LTD]11 package rows20220312_118078fc-2cfe-4b82-8a21-026c17d1acd6.zip

Reported adverse events (FAERS/openFDA)#

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