NDC 86217-0011-1 - FENBENPRO PURITY and PRECISION 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
- 86217-0011
- Requested NDC
- 86217-0011-1
- Package NDCs from labels
- 86217-0011-1
- Manufacturer
- HUBIHOL, UAB
- Effective date
- 2025-03-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| FENBENPRO PURITY and PRECISION FENBENDAZOLE - HUBIHOL, UAB | HUBIHOL, UAB | 2025-03-03 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86217-0011-1 | FENBENPRO PURITY and PRECISION FENBENDAZOLE | 180 U in 1 PACKAGE | CAPSULE | 180 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 86217-0011 | FENBENPRO PURITY AND PRECISION FENBENDAZOLE CAPSULE [HUBIHOL, UAB] | 1 | 1 package rows | 20250305_35750e2b-fb13-4a67-aa10-4e0fc496d870.zip |
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 |
|---|---|---|---|---|---|---|
| PREPAKU FENBENDAZOLE Canine Dewormer | FENBENDAZOLE | Shenzhen Zhenshangzekai Technology Co., Ltd. | 4d722051-6a49-75ea-e063-6294a90a7b4e | 2026-03-20 | Warnings | 621BVT9M36 |
| 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.