NDC 0010-4120 - NexGard COMBO
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
- 0010-4120
- Package NDCs from labels
- 0010-4120-01, 0010-4120-02, 0010-4120-03
- Manufacturer
- Boehringer Ingelheim Animal Health USA Inc.
- Effective date
- 2026-07-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| NexGard® COMBO (esafoxalaner, eprinomectin, and praziquantel topical solution) | Boehringer Ingelheim Animal Health USA Inc. | 2026-07-17 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0010-4120-01 | NexGard COMBO | 0.3 mL in 1 APPLICATOR | SOLUTION | 0.3 | 5 | |
| 0010-4120-01 | NexGard COMBO | 1 in 1 CARTON | SOLUTION | 1 | 5 | |
| 0010-4120-02 | NexGard COMBO | 0.3 mL in 1 APPLICATOR | SOLUTION | 0.3 | 5 | |
| 0010-4120-02 | NexGard COMBO | 3 in 1 CARTON | SOLUTION | 3 | 5 | |
| 0010-4120-03 | NexGard COMBO | 6 in 1 CARTON | SOLUTION | 6 | 5 | |
| 0010-4120-03 | NexGard COMBO | 0.3 mL in 1 APPLICATOR | SOLUTION | 0.3 | 5 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| PRAZIQUANTEL | PRAZIQUANTEL | Par Health USA, LLC | 16f2b9c4-a260-4a31-bd52-e5945913246c | 2026-08-12 | Warnings, Adverse reactions | 6490C9U457 |
| Biltricide | PRAZIQUANTEL | Bayer HealthCare Pharmaceuticals Inc. | 34ce1cdd-648e-4f1e-8512-bf3d4cc22eb9 | 2026-03-02 | Warnings, Adverse reactions | 6490C9U457 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.