NDC 57926-474-20 - Panacur
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
- 57926-474
- Requested NDC
- 57926-474-20
- Package NDCs from labels
- 57926-474-20
- Manufacturer
- Merck Sharp & Dohme Corp.
- Effective date
- 2026-05-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| panacur ® (fenbendazole) | Merck Sharp & Dohme Corp. | 2026-05-19 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 57926-474-20 | Panacur | 454 g in 1 JAR | GRANULE | 454 | 6 | |
| 57926-474-20 | Panacur | 1 in 1 CARTON | GRANULE | 1 | 6 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| FENBENDAZOLE | ACTIVE INGREDIENT | 621BVT9M36 | PANACUR (FENBENDAZOLE) GRANULE [MERCK SHARP & DOHME CORP.] | 1 | |
| FENBENDAZOLE | ACTIVE MOIETY | 621BVT9M36 | PANACUR (FENBENDAZOLE) GRANULE [MERCK SHARP & DOHME CORP.] | 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 |
|---|---|---|---|---|---|---|
| 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.