NDC 17033-002-01 - Solovecin
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
- 17033-002
- Requested NDC
- 17033-002-01
- Package NDCs from labels
- 17033-002-01
- Manufacturer
- Dechra Veterinary Products, LLC
- Effective date
- 2025-09-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Solovecin - Dechra Veterinary Products, LLC | Dechra Veterinary Products, LLC | 2025-09-03 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17033-002-01 | Solovecin | 1 in 1 CARTON | INJECTION, POWDER, LYOPHILIZED, | 1 | 1 | |
| 17033-002-01 | Solovecin | 10 mL in 1 VIAL, MULTI-DOSE | INJECTION, POWDER, LYOPHILIZED, | 10 | 1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.