FDA.reportPublic FDA data

NDC 70748-450 - risperidone

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
70748-450
Package NDCs from labels
70748-450-11
Manufacturer
Lupin Pharmaceuticals, Inc.
Effective date
2026-02-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
risperidone - Lupin Pharmaceuticals, Inc.Lupin Pharmaceuticals, Inc.2026-02-24HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70748-450-11risperidone2 mL in 1 VIALINJECTION, POWDER, FOR SUSPENSIO2 mL37.5 mg in 2mL4