FDA.reportPublic FDA data

Trilostane

Manufacturer
H3 Medical Inc
Effective date
2017-12-04
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
1
Source
full-release
Hydrated at
2026-06-01 02:48:41

Label at a glance#

ProductTrilostane
Active ingredientTRILOSTANE
Label structure1 sections

Label contents#

Full prescribing information#

Package Label 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TrilostaneTrilostane

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63732-2018-4Trilostane100 g in 1 BOTTLEPOWDER1001
63732-2018-5Trilostane500 g in 1 BOTTLEPOWDER5001
63732-2018-6Trilostane1000 g in 1 BOTTLEPOWDER10001
63732-2018-7Trilostane5000 g in 1 PAILPOWDER50001
63732-2018-8Trilostane10000 g in 1 DRUMPOWDER100001
63732-2018-9Trilostane25000 g in 1 DRUMPOWDER250001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63732-2018TRILOSTANE POWDER [H3 MEDICAL INC]16 package rows20171204_968a5b95-1a2e-45a0-b589-0342d2bbcaeb.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
63732-201863732-2018-4, 63732-2018-5, 63732-2018-6, 63732-2018-7, 63732-2018-8, 63732-2018-9

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.