FDA.reportPublic FDA data

NDC 70710-2090 - BEIZRAY

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
70710-2090
Package NDCs from labels
70710-2090-1
Manufacturer
Zydus Pharmaceuticals USA Inc. | Kindos Pharmaceuticals Co., Ltd. | Ningbo Shuangcheng Pharmaceutical Co., Ltd | Bio Products Laboratory Ltd.
Effective date
2025-12-17
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
BEIZRAYZydus Pharmaceuticals USA Inc. | Kindos Pharmaceuticals Co., Ltd. | Ningbo Shuangcheng Pharmaceutical Co., Ltd | Bio Products Laboratory Ltd.2025-12-17HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70710-2090-1BEIZRAY4 mL in 1 VIAL, GLASSINJECTION, SOLUTION4 mL20 mg in 1mL4
70710-2090-1BEIZRAY4 mL in 1 VIAL, GLASSINJECTION, SOLUTION4 mL20 mg in 1mL4