NDC 55529-181-34 - Enroflox
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
- 55529-181
- Requested NDC
- 55529-181-34
- Package NDCs from labels
- 55529-181-26, 55529-181-34
- Manufacturer
- Norbrook Laboratories Limited
- Effective date
- 2026-07-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Enroflox - Norbrook Laboratories Limited | Norbrook Laboratories Limited | 2026-07-01 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55529-181-26 | Enroflox | 50 in 1 BOTTLE, PLASTIC | TABLET, CHEWABLE | 50 | 2 | |
| 55529-181-34 | Enroflox | 200 in 1 BOTTLE, PLASTIC | TABLET, CHEWABLE | 200 | 2 |
DailyMed Dashboard NDC Coverage#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.