NDC 0061-1440-03 - Exzolt
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
- 0061-1440
- Requested NDC
- 0061-1440-03
- Package NDCs from labels
- 0061-1440-01, 0061-1440-02, 0061-1440-03
- Manufacturer
- Merck Sharp & Dohme Corp.
- Effective date
- 2026-08-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Exzolt ® (fluralaner oral solution) | Merck Sharp & Dohme Corp. | 2026-08-25 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0061-1440-01 | Exzolt | 1 mL in 1 BOTTLE, PLASTIC | SOLUTION | 1 | 6 | |
| 0061-1440-02 | Exzolt | 4 mL in 1 BOTTLE, PLASTIC | SOLUTION | 4 | 6 | |
| 0061-1440-03 | Exzolt | 4 mL in 1 BOTTLE, GLASS | SOLUTION | 4 | 6 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.