FDA.reportPublic FDA data

NDC 23243-0064 - Monovet 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
23243-0064
Package NDCs from labels
23243-0064-5, 23243-0064-9
Manufacturer
Huvepharma, Inc. | Huvepharma EOOD | Huvepharma, Inc
Effective date
2024-07-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Monovet 90 - Huvepharma, Inc. | Huvepharma EOOD | Huvepharma, IncHuvepharma, Inc. | Huvepharma EOOD | Huvepharma, Inc2024-07-09OTC TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23243-0064-5Monovet 9025 kg in 1 BAGGRANULE257
23243-0064-9Monovet 90500 kg in 1 SUPERSACKGRANULE5007

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
23243-0064MONOVET 90 (MONENSIN TYPE A MEDICATED ARTICLE) GRANULE [HUVEPHARMA, INC.]72 package rows20240723_93180485-e5be-4ee3-8f61-3a250761a542.zip

Reported adverse events (FAERS/openFDA)#

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