FDA.reportPublic FDA data

Detomidine HCl

Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2022-03-11
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
1
Source
full-release
Hydrated at
2026-06-01 02:50:24

Label at a glance#

ProductDetomidine HCl
Active ingredientDETOMIDINE HYDROCHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

Detomidine HCl

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73309-36473309-364-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
DETOMIDINE HYDROCHLORIDE95K4LKB6QEACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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