NDC 86101-069-14 - Firocoxib
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
- 86101-069
- Requested NDC
- 86101-069-14
- Package NDCs from labels
- 86101-069-60, 86101-069-14, 86101-069-06
- Manufacturer
- FELIX PHARMACEUTICALS PRIVATE LIMITED
- Effective date
- 2026-03-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Firocoxib - FELIX PHARMACEUTICALS PRIVATE LIMITED | FELIX PHARMACEUTICALS PRIVATE LIMITED | 2026-03-05 | Prescription Animal Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86101-069-06 | Firocoxib | 3 in 1 CARTON | TABLET, CHEWABLE | 3 | 1 | |
| 86101-069-06 | Firocoxib | 10 in 1 BLISTER PACK | TABLET, CHEWABLE | 10 | 1 | |
| 86101-069-14 | Firocoxib | 180 in 1 BOTTLE | TABLET, CHEWABLE | 180 | 1 | |
| 86101-069-60 | Firocoxib | 60 in 1 BOTTLE | TABLET, CHEWABLE | 60 | 1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.