NDC 86241-115 - OZIPCO DEWORMER FENBENDAZOLE
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
- 86241-115
- Package NDCs from labels
- 86241-115-01
- Manufacturer
- Fast Sold LLC
- Effective date
- 2026-09-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| OZIPCO DEWORMER FENBENDAZOLE - Fast Sold LLC | Fast Sold LLC | 2026-09-25 | OTC ANIMAL DRUG LABEL |
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 |
|---|---|---|---|---|---|---|
| Fenbendazole 222 MG | FENBENDAZOLE 222 MG | B & L Healthcare Products INC | 337c4554-2049-a725-e063-6394a90a66f5 | 2025-04-23 | Warnings | 621BVT9M36 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.