NDC 61133-4005 - Eprimectin
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
- 61133-4005
- Package NDCs from labels
- 61133-4005-3, 61133-4005-4, 61133-4005-5
- Manufacturer
- Bimeda, Inc.
- Effective date
- 2026-01-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Eprimectin TM Pour-On (eprinomectin) | Bimeda, Inc. | 2026-01-21 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 61133-4005-3 | Eprimectin | 2500 mL in 1 BOTTLE, PLASTIC | SOLUTION | 2500 | 1 | |
| 61133-4005-4 | Eprimectin | 5000 mL in 1 BOTTLE, PLASTIC | SOLUTION | 5000 | 1 | |
| 61133-4005-5 | Eprimectin | 10000 mL in 1 BOTTLE, PLASTIC | SOLUTION | 10000 | 1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.