Home NDC 63732-2018-9 NDC 63732-2018-9 - 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 63732-2018
Requested NDC 63732-2018-9
Package NDCs from labels 63732-2018-4, 63732-2018-5, 63732-2018-6, 63732-2018-7, 63732-2018-8, 63732-2018-9
Manufacturer H3 Medical Inc
Effective date 2017-12-04
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Trilostane - H3 Medical Inc H3 Medical Inc 2017-12-04 BULK INGREDIENT - ANIMAL DRUG
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63732-2018-4 Trilostane 100 g in 1 BOTTLE POWDER 100 1 63732-2018-5 Trilostane 500 g in 1 BOTTLE POWDER 500 1 63732-2018-6 Trilostane 1000 g in 1 BOTTLE POWDER 1000 1 63732-2018-7 Trilostane 5000 g in 1 PAIL POWDER 5000 1 63732-2018-8 Trilostane 10000 g in 1 DRUM POWDER 10000 1 63732-2018-9 Trilostane 25000 g in 1 DRUM POWDER 25000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63732-2018 TRILOSTANE POWDER [H3 MEDICAL INC] 1 6 package rows 20171204_968a5b95-1a2e-45a0-b589-0342d2bbcaeb.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.