FDA.reportPublic FDA data

NDC 23243-2309-3 - CORID

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
23243-2309
Requested NDC
23243-2309-3
Package NDCs from labels
23243-2309-3
Manufacturer
Huvepharma, Inc | Huvepharma EOOD | Huvepharma Inc
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
CORID - Huvepharma, Inc | Huvepharma EOOD | Huvepharma IncHuvepharma, Inc | Huvepharma EOOD | Huvepharma Inc2024-10-31OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23243-2309-3CORID283.5 g in 1 POUCHPOWDER, FOR SOLUTION283.55

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
23243-2309CORID (AMPROLIUM) POWDER, FOR SOLUTION [HUVEPHARMA, INC]51 package rows20241105_b297cc2e-8b96-41d1-a132-d68ccb1326b3.zip

Reported adverse events (FAERS/openFDA)#

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