NDC 58198-2113-1 - Rumensin 113
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
- 58198-2113
- Requested NDC
- 58198-2113-1
- Package NDCs from labels
- 58198-2113-1, 58198-2113-2, 58198-2113-3
- Manufacturer
- Elanco US Inc.
- Effective date
- 2026-04-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Rumensin 113 - Elanco US Inc. | Elanco US Inc. | 2026-04-21 | OTC TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 58198-2113-1 | Rumensin 113 | 25 kg in 1 BAG | GRANULE | 25 | 1 | |
| 58198-2113-2 | Rumensin 113 | 600 kg in 1 BAG | GRANULE | 600 | 1 | |
| 58198-2113-3 | Rumensin 113 | 900 kg in 1 BAG | GRANULE | 900 | 1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.