NDC 17033-009-04 - Emeprev
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
- 17033-009
- Requested NDC
- 17033-009-04
- Package NDCs from labels
- 17033-009-04, 17033-009-60
- Manufacturer
- Dechra Vet Products, LLC
- Effective date
- 2026-02-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Emeprev - Dechra Vet Products, LLC | Dechra Vet Products, LLC | 2026-02-12 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17033-009-04 | Emeprev | 1 in 1 CARTON | TABLET | 1 | 2 | |
| 17033-009-04 | Emeprev | 4 in 1 BLISTER PACK | TABLET | 4 | 2 | |
| 17033-009-60 | Emeprev | 60 in 1 BOTTLE | TABLET | 60 | 2 |
DailyMed Dashboard NDC Coverage#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.