Home NDC 69182-004 NDC 69182-004 - 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 69182-004
Package NDCs from labels 69182-004-05, 69182-004-01
Manufacturer Zhejiang Xianju Junye Pharmaceutical Co., Ltd | Zhejiang Xianju Junye Pharmaceutical Co., Ltd.
Effective date 2023-11-14
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Trilostane Zhejiang Xianju Junye Pharmaceutical Co., Ltd | Zhejiang Xianju Junye Pharmaceutical Co., Ltd. 2023-11-14 BULK INGREDIENT - ANIMAL DRUG Trilostane Zhejiang Xianju Junye Pharmaceutical Co., Ltd | Zhejiang Xianju Junye Pharmaceutical Co., Ltd. 2023-11-14 BULK INGREDIENT - ANIMAL DRUG
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69182-004-01 Trilostane 1 kg in 1 DRUM POWDER 1 1 69182-004-05 Trilostane 5 kg in 1 DRUM POWDER 5 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69182-004 TRILOSTANE POWDER [ZHEJIANG XIANJU JUNYE PHARMACEUTICAL CO., LTD] 1 1 package rows 20231115_f1244915-7364-4e7e-8f37-666eaf220b6b.zip 69182-004 TRILOSTANE POWDER [ZHEJIANG XIANJU JUNYE PHARMACEUTICAL CO., LTD] 1 1 package rows 20231118_9c7582af-3cf9-4a81-b220-3b439dc5132e.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.