NDC 50604-9150-1 - PREVICOX
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
- 50604-9150
- Requested NDC
- 50604-9150-1
- Package NDCs from labels
- 50604-9150-1, 50604-9150-2, 50604-9150-3, 50604-9150-4, 50604-9150-5, 50604-9150-6
- Manufacturer
- Merial, Inc. | Boehringer Ingelheim Animal Health USA Inc.
- Effective date
- 2020-04-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PREVICOX ® (firocoxib) Chewable Tablets | Merial, Inc. | Boehringer Ingelheim Animal Health USA Inc. | 2020-04-17 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| FIROCOXIB | ACTIVE INGREDIENT | Y6V2W4S4WT | PREVICOX (FIROCOXIB) TABLET, CHEWABLE [MERIAL LIMITED] | 3 | |
| FIROCOXIB | ACTIVE MOIETY | Y6V2W4S4WT | PREVICOX (FIROCOXIB) TABLET, CHEWABLE [MERIAL LIMITED] | 3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.