FDA.reportPublic FDA data

NDC 23243-9709-3 - Amprol 128

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
23243-9709
Requested NDC
23243-9709-3
Package NDCs from labels
23243-9709-3
Manufacturer
Huvepharma, Inc. | Huvepharma EOOD
Effective date
2024-10-31
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Amprol 128 - Huvepharma, Inc. | Huvepharma EOODHuvepharma, Inc. | Huvepharma EOOD2024-10-31OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23243-9709-3Amprol128283.5 g in 1 POUCHPOWDER283.57

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
23243-9709AMPROL 128 (AMPROLIUM) POWDER [HUVEPHARMA, INC.]71 package rows20241103_ccf7a5cc-b50a-4dc4-8de8-13c9e36608cb.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AMPROLIUMACTIVE INGREDIENT95CO6N199QAMPROL 128 (AMPROLIUM) POWDER [HUVEPHARMA, INC.]3
AMPROLIUMACTIVE MOIETY95CO6N199QAMPROL 128 (AMPROLIUM) POWDER [HUVEPHARMA, INC.]3

Reported adverse events (FAERS/openFDA)#

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