NDC 86197-005-02 - 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
- 86197-005
- Requested NDC
- 86197-005-02
- Package NDCs from labels
- 86197-005-01, 86197-005-02, 86197-005-03
- Manufacturer
- Hunan Huateng Pharma Tech Co., Ltd.
- Effective date
- 2026-08-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Trilostane - Hunan Huateng Pharma Tech Co., Ltd. | Hunan Huateng Pharma Tech Co., Ltd. | 2026-08-21 | BULK INGREDIENT - ANIMAL DRUG |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86197-005-01 | Trilostane | 1000 g in 1 BAG | POWDER | 1000 | 2 | |
| 86197-005-02 | Trilostane | 500 g in 1 BAG | POWDER | 500 | 2 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.