FDA.reportPublic FDA data

NDC 23243-6681-2 - Amprol

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
23243-6681
Requested NDC
23243-6681-2
Package NDCs from labels
23243-6681-2
Manufacturer
Huvepharma, Inc | Huvepharma EOOD
Effective date
2026-05-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Amprol - Huvepharma, Inc | Huvepharma EOODHuvepharma, Inc | Huvepharma EOOD2026-05-21OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23243-6681-2Amprol3785 mL in 1 BOTTLE, PLASTICSOLUTION37859
23243-6681-2Amprol4 in 1 BOXSOLUTION49

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
23243-6681AMPROL (AMPROLIUM) SOLUTION [HUVEPHARMA, INC]82 package rows20250215_831141f7-9458-4de5-9ddc-d183e220fbb7.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AMPROLIUMACTIVE INGREDIENT95CO6N199QAMPROL (AMPROLIUM) SOLUTION [HUVEPHARMA, INC.]3
AMPROLIUMACTIVE MOIETY95CO6N199QAMPROL (AMPROLIUM) SOLUTION [HUVEPHARMA, INC.]3
WATERINACTIVE INGREDIENT059QF0KO0RAMPROL (AMPROLIUM) SOLUTION [HUVEPHARMA, INC.]3

Reported adverse events (FAERS/openFDA)#

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