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
Contacts and useful links#
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
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 38779-2387-3 | GM - Gram | 38779-2387 | 487345ab-7a05-4f27-9c9e-537194c607cd | 1 | 2015-10-02 |
| 38779-2387-4 | GM - Gram | 38779-2387 | f646def8-6193-404f-bcb8-7aec02d73d65 | 1 | 2015-10-02 |
| 38779-2387-5 | GM - Gram | 38779-2387 | ed26e460-9ad2-4ff7-a718-aa56f63ed980 | 1 | 2015-10-02 |
| 38779-2387-8 | GM - Gram | 38779-2387 | 7bcce813-0447-47e1-a707-533408e49976 | 1 | 2015-10-02 |
| 38779-2387-9 | GM - Gram | 38779-2387 | 48808c66-e685-4cf3-b186-868bcf08aca2 | 1 | 2015-10-02 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| TRILOSTANE | ACTIVE INGREDIENT | L0FPV48Q5R | 3 | |
| TRILOSTANE | ACTIVE MOIETY | L0FPV48Q5R | 3 |
Products#
Every source-derived product name is available through these pages.
- Trilostane
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 38779-2387 | 38779-2387-3, 38779-2387-4, 38779-2387-5, 38779-2387-8, 38779-2387-9 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| TRILOSTANE | L0FPV48Q5R | ACTIM |
Source Document#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
