FDA.reportPublic FDA data

NDC 0480-9733 - 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
0480-9733
Package NDCs from labels
0480-9733-01
Manufacturer
Teva Pharmaceuticals, Inc.
Effective date
2025-02-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Risperidone - Teva Pharmaceuticals, Inc.Teva Pharmaceuticals, Inc.2025-02-28HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0480-9733-01Risperidone2 mL in 1 VIALINJECTION, POWDER, FOR SUSPENSIO2 mL25 mg in 2mL3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0480-9733RISPERIDONE KIT [TEVA PHARMACEUTICALS, INC.]3Unmatched20250402_32c0f081-b418-4c1c-b39e-eb5c344043c7.zip