NDC 86212-001-07 - 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
- 86212-001
- Requested NDC
- 86212-001-07
- Package NDCs from labels
- 86212-001-06, 86212-001-07, 86212-001-08, 86212-001-01, 86212-001-03, 86212-001-02, 86212-001-05
- Manufacturer
- Liaoning Pharmaceutical Innovation Co., Ltd.
- Effective date
- 2025-12-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Trilostane | Liaoning Pharmaceutical Innovation Co., Ltd. | 2025-12-08 | BULK INGREDIENT - ANIMAL DRUG |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86212-001-01 | Trilostane | 0.01 kg in 1 BAG | POWDER | 0.01 | 3 | |
| 86212-001-02 | Trilostane | 0.05 kg in 1 BAG | POWDER | 0.05 | 3 | |
| 86212-001-03 | Trilostane | 0.1 kg in 1 BAG | POWDER | 0.1 | 3 | |
| 86212-001-05 | Trilostane | 0.5 kg in 1 BAG | POWDER | 0.5 | 3 | |
| 86212-001-06 | Trilostane | 1 kg in 1 BAG | POWDER | 1 | 3 | |
| 86212-001-07 | Trilostane | 5 kg in 1 BAG | POWDER | 5 | 3 | |
| 86212-001-08 | Trilostane | 10 kg in 1 BAG | POWDER | 10 | 3 |
DailyMed Dashboard NDC Coverage#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.