FDA.reportPublic FDA data

NDC 69238-2792 - Naltrexone

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
69238-2792
Package NDCs from labels
69238-2792-1
Manufacturer
Amneal Pharmaceuticals NY LLC | Alkermes, Inc
Effective date
2026-01-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Naltrexone - Amneal Pharmaceuticals NY LLC | Alkermes, IncAmneal Pharmaceuticals NY LLC | Alkermes, Inc2026-01-30HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69238-2792-1Naltrexone5 mL in 1 VIAL, GLASSINJECTION, POWDER, FOR SUSPENSIO5 mL380 mg in 5mL1