FDA.reportPublic FDA data

TRILOSTANE

Manufacturer
PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC
Effective date
2021-03-11
Label type
BULK INGREDIENT
Version
2
Source
full-release
Hydrated at
2026-06-01 02:49:54

Label at a glance#

ProductTRILOSTANE
Active ingredientTRILOSTANE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

trilostanelabel.jpgPACKAGE LABEL IMAGEPACKAGE LABEL IMAGE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72969-074-10TRILOSTANE1 g in 1 PACKAGEPOWDER12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72969-074TRILOSTANE POWDER [PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC]21 package rows20210312_18bdb7f5-b147-4b2c-90cb-e3498aaa6554.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
72969-07472969-074-10

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.