FDA.reportPublic FDA data

NDC 73377-027-01 - 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
73377-027
Requested NDC
73377-027-01
Package NDCs from labels
73377-027-01, 73377-027-02, 73377-027-03
Manufacturer
AX Pharmaceutical Corp
Effective date
2024-10-22
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Trilostane - AX Pharmaceutical CorpAX Pharmaceutical Corp2024-10-22BULK INGREDIENT - ANIMAL DRUG

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

Reported adverse events (FAERS/openFDA)#

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