NDC 86101-002-16 - Enrofloxacin Flavored
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
- 86101-002
- Requested NDC
- 86101-002-16
- Package NDCs from labels
- 86101-002-50, 86101-002-16
- Manufacturer
- FELIX PHARMACEUTICALS PRIVATE LIMITED
- Effective date
- 2026-02-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Enrofloxacin Flavored - FELIX PHARMACEUTICALS PRIVATE LIMITED | FELIX PHARMACEUTICALS PRIVATE LIMITED | 2026-02-24 | Prescription Animal Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86101-002-16 | EnrofloxacinFlavored | 250 in 1 BOTTLE | TABLET | 250 | 5 | |
| 86101-002-50 | EnrofloxacinFlavored | 50 in 1 BOTTLE | TABLET | 50 | 5 |
DailyMed Dashboard NDC Coverage#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.