FDA.reportPublic FDA data

NDC 71052-525 - Trilostane

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
71052-525
Package NDCs from labels
71052-525-01, 71052-525-10, 71052-525-15, 71052-525-00, 71052-525-05
Manufacturer
DARMERICA, LLC
Effective date
2026-10-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Trilostane - DARMERICA, LLCDARMERICA, LLC2026-10-07BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-525-00Trilostane1 kg in 1 PACKAGEPOWDER16
71052-525-01Trilostane0.01 kg in 1 PACKAGEPOWDER0.016
71052-525-05Trilostane0.05 kg in 1 PACKAGEPOWDER0.056
71052-525-10Trilostane0.1 kg in 1 PACKAGEPOWDER0.16
71052-525-15Trilostane0.5 kg in 1 PACKAGEPOWDER0.56

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71052-525TRILOSTANE POWDER [DARMERICA, LLC]55 package rows20240510_fac292e4-e1b1-44f4-9f0f-9953dd1f1c37.zip

Reported adverse events (FAERS/openFDA)#

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