FDA.reportPublic FDA data

NDC 58198-1825 - Rumensin 90

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
58198-1825
Package NDCs from labels
58198-1825-1, 58198-1825-2, 58198-1825-3
Manufacturer
Elanco US Inc. | Elanco Clinton Laboratories
Effective date
2021-08-04
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Rumensin 90 - Elanco US Inc. | Elanco Clinton LaboratoriesElanco US Inc. | Elanco Clinton Laboratories2021-08-04OTC TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58198-1825-1Rumensin 9025 kg in 1 BAGGRANULE259
58198-1825-2Rumensin 90600 kg in 1 BAGGRANULE6009
58198-1825-3Rumensin 90900 kg in 1 BAGGRANULE9009

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58198-1825RUMENSIN 90 (MONENSIN) GRANULE [ELANCO US INC.]93 package rows20210811_3e6db03e-55d5-4802-b0d2-3bc566e976b2.zip

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.