FDA.reportPublic FDA data

Trilostane

Manufacturer
AX Pharmaceutical Corp
Effective date
2024-10-22
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 20:51:20

Label at a glance#

ProductTrilostane
Active ingredientTRILOSTANE
Label structure1 sections

Label contents#

Full prescribing information#

Trilostane

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage descriptionimage descriptionimage description

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73377-027TRILOSTANE POWDER [AX PHARMACEUTICAL CORP]5Unmatched20241025_6fef97de-f7b3-4e19-ae9e-668a7452446c.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73377-02773377-027-01, 73377-027-02, 73377-027-03

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
TRILOSTANEL0FPV48Q5RACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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