NDC 50604-6597-1 - EQUIOXX
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
- 50604-6597
- Requested NDC
- 50604-6597-1
- Package NDCs from labels
- 50604-6597-1, 50604-6597-2
- Manufacturer
- Merial, Inc.
- Effective date
- 2018-12-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Equioxx ® (firocoxib) Oral Paste for Horses | Merial, Inc. | 2018-12-12 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| firocoxib | ACTIVE INGREDIENT | Y6V2W4S4WT | EQUIOXX (FIROCOXIB) PASTE [MERIAL LIMITED] | 2 | |
| firocoxib | ACTIVE MOIETY | Y6V2W4S4WT | EQUIOXX (FIROCOXIB) PASTE [MERIAL LIMITED] | 2 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.