Trilostane

Manufacturer
Medisca Inc.
Effective date
2021-10-25
Label type
BULK INGREDIENT
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 22:30:48

Label at a glance#

ProductTrilostane
Active ingredientTRILOSTANE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESCRIPTION: Off-white to white powder with weak odor.

NDC: 38779-2387-5

Packed by Medisca Inc.
Plattsburgh, NY, 12901, USA

MEDISCA

TO ORDER CALL 1 (800) 932-1039

TRILOSTANE

Caution: Not for Human Use

100 g

For use and distribution in prescription compounding, manufacturing, processing or repacking only in accordance with FDA regulations and applicable law.

STORAGE: Preserve in tight containers.

Lot:

Exp:

Cas: 13647-35-3

See Material Safety Data Sheet

image of labelimage of label

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
38779-2387-3GM - Gram38779-2387487345ab-7a05-4f27-9c9e-537194c607cd12015-10-02
38779-2387-4GM - Gram38779-2387f646def8-6193-404f-bcb8-7aec02d73d6512015-10-02
38779-2387-5GM - Gram38779-2387ed26e460-9ad2-4ff7-a718-aa56f63ed98012015-10-02
38779-2387-8GM - Gram38779-23877bcce813-0447-47e1-a707-533408e4997612015-10-02
38779-2387-9GM - Gram38779-238748808c66-e685-4cf3-b186-868bcf08aca212015-10-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
TRILOSTANEACTIVE INGREDIENTL0FPV48Q5R3
TRILOSTANEACTIVE MOIETYL0FPV48Q5R3

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
38779-238738779-2387-3, 38779-2387-4, 38779-2387-5, 38779-2387-8, 38779-2387-9

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
TRILOSTANEL0FPV48Q5RACTIM

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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