NDC 86184-395 - TRICLABENDAZOLE
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
- 86184-395
- Package NDCs from labels
- 86184-395-01
- Manufacturer
- MAEDA INC
- Effective date
- 2026-04-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| TRICLABENDAZOLE - MAEDA INC | MAEDA INC | 2026-04-13 | BULK INGREDIENT - ANIMAL DRUG |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86184-395-01 | TRICLABENDAZOLE | 1 g in 1 PACKAGE | POWDER | 1 | 1 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| EGATEN | TRICLABENDAZOLE | Novartis Pharmaceuticals Corporation | 5552884e-10ea-450c-9658-d3d4f33c946e | 2026-06-04 | Warnings, Adverse reactions | 4784C8E03O |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.