FDA.reportPublic FDA data

NDC 86122-001-26 - 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
86122-001
Requested NDC
86122-001-26
Package NDCs from labels
86122-001-26, 86122-001-27, 86122-001-28, 86122-001-29, 86122-001-21, 86122-001-20, 86122-001-22, 86122-001-01, 86122-001-02, 86122-001-03, 86122-001-04, 86122-001-05
Manufacturer
Tianjin Pharmaceutical Innovation Co., Ltd.
Effective date
2023-01-04
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
TrilostaneTianjin Pharmaceutical Innovation Co., Ltd.2023-01-04BULK INGREDIENT - ANIMAL DRUG
TrilostaneTianjin Pharmaceutical Innovation Co., Ltd.2022-08-07BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86122-001-20Trilostane0.05 kg in 1 BAGPOWDER0.052
86122-001-21Trilostane0.1 kg in 1 BAGPOWDER0.12
86122-001-22Trilostane0.5 kg in 1 BAGPOWDER0.52
86122-001-26Trilostane1 kg in 1 BAGPOWDER12
86122-001-27Trilostane5 kg in 1 BAGPOWDER52
86122-001-28Trilostane10 kg in 1 BAGPOWDER102
86122-001-29Trilostane0.01 kg in 1 BAGPOWDER0.012

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86122-001TRILOSTANE POWDER [TIANJIN PHARMACEUTICAL INNOVATION CO., LTD.]27 package rows20230106_a4c66825-2546-435e-8fa7-dbd29e77d15f.zip

Reported adverse events (FAERS/openFDA)#

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