NDC 51072-116 - EquiCoxib
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
- 51072-116
- Package NDCs from labels
- 51072-116-00, 51072-116-01
- Manufacturer
- Aurora Pharmaceutical, Inc.
- Effective date
- 2025-12-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| EquiCoxib™ (firocoxib) Oral Solution for Horses | Aurora Pharmaceutical, Inc. | 2025-12-11 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51072-116-00 | EquiCoxib | 1 in 1 CARTON | SOLUTION | 1 | 3 | |
| 51072-116-00 | EquiCoxib | 90 mL in 1 BOTTLE | SOLUTION | 90 | 3 | |
| 51072-116-01 | EquiCoxib | 400 mL in 1 BOTTLE | SOLUTION | 400 | 3 | |
| 51072-116-01 | EquiCoxib | 1 in 1 CARTON | SOLUTION | 1 | 3 |
DailyMed Dashboard NDC Coverage#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.