FDA.reportPublic FDA data

Trilostane

Manufacturer
AX Pharmaceutical Corp
Effective date
2019-10-25
Label type
BULK INGREDIENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:49:24

Label at a glance#

ProductTrilostane
Active ingredientTRILOSTANE
Label structure1 sections

Label contents#

Full prescribing information#

Trilostane

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62157-927-01Trilostane100 g in 1 JARPOWDER1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62157-927TRILOSTANE POWDER [AX PHARMACEUTICAL CORP]11 package rows20191026_03dc4d08-45a2-4982-a31f-d36afa76868c.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
62157-92762157-927-01

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
TRILOSTANEL0FPV48Q5RACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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