Home NDC 58198-1372 NDC 58198-1372 - Maxiban 72 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 58198-1372
Package NDCs from labels 58198-1372-1
Manufacturer Elanco US Inc.
Effective date 2026-05-20
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Maxiban 72 - Elanco US Inc. Elanco US Inc. 2026-05-20 OTC TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58198-1372-1 Maxiban 72 25 kg in 1 BAG POWDER 25 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58198-1372 MAXIBAN 72 (NARASIN AND NICARBAZIN) POWDER [ELANCO US INC.] 6 1 package rows 20240606_fa5d5382-280d-48f2-8105-304bb6a0f284.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.