FDA.reportPublic FDA data

NDC 70121-1350 - 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
70121-1350
Package NDCs from labels
70121-1350-1
Manufacturer
Amneal Pharmaceuticals LLC | Amneal Pharmaceuticals Private Limited
Effective date
2025-07-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
DILUENT - Amneal Pharmaceuticals LLC | Amneal Pharmaceuticals Private LimitedAmneal Pharmaceuticals LLC | Amneal Pharmaceuticals Private Limited2025-07-06HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70121-1350-1Risperidone2 mL in 1 VIALINJECTION, POWDER, FOR SUSPENSIO2 mL12.5 mg in 2mL6