NDC 50604-7314 - Marquis Antiprotozoal
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
- 50604-7314
- Package NDCs from labels
- 50604-7314-1, 50604-7314-2
- Manufacturer
- Merial, Inc.
- Effective date
- 2021-12-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Marquis ® (15% w/w ponazuril) | Merial, Inc. | 2021-12-30 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| ponazuril | ACTIVE INGREDIENT | JPW84AS66U | MARQUIS ANTIPROTOZOAL (PONAZURIL) PASTE [MERIAL, INC.] | 1 | |
| ponazuril | ACTIVE MOIETY | JPW84AS66U | MARQUIS ANTIPROTOZOAL (PONAZURIL) PASTE [MERIAL, INC.] | 1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.