NDC 86136-163-36 - OstiCoxib EQ
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
- 86136-163
- Requested NDC
- 86136-163-36
- Package NDCs from labels
- 86136-163-35, 86136-163-36, 86136-163-65
- Manufacturer
- MWI/Vetone | FELIX PHARMACEUTICALS PRIVATE LIMITED
- Effective date
- 2026-09-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| OstiCoxib EQ - MWI/Vetone | FELIX PHARMACEUTICALS PRIVATE LIMITED | MWI/Vetone | FELIX PHARMACEUTICALS PRIVATE LIMITED | 2026-09-29 | Prescription Animal Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86136-163-35 | OstiCoxib EQ | 30 in 1 BLISTER PACK | TABLET, CHEWABLE | 30 | 1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.