PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Trilostane
- Manufacturer
- AMERICAN PHARMACEUTICAL INGREDIENTS LLC | LUMIS GLOBAL PHARMACEUTICALS CO LTD
- Effective date
- 2014-03-26
- Label type
- BULK INGREDIENT
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:47:53
Label at a glance#
ProductTrilostane
Active ingredientTrilostane
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 58597-7038-6 | Trilostane | 100 g in 1 BOTTLE | POWDER | 100 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 58597-7038 | TRILOSTANE POWDER [AMERICAN PHARMACEUTICAL INGREDIENTS LLC] | 2 | 1 package rows | 20140326_9ca51c60-3376-48c7-b80b-082c2bcccdd5.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Trilostane | ACTIVE INGREDIENT | L0FPV48Q5R | 2 | |
| TRILOSTANE | ACTIVE MOIETY | L0FPV48Q5R | 2 |
Products#
Every source-derived product name is available through these pages.
- Trilostane
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 58597-7038 | 58597-7038-6 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Trilostane | L0FPV48Q5R | ACTIB |
Source Document#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.