# CUVITRU

NDC: 0944-2850
Generic name: Immune Globulin Subcutaneous (Human)
Labeler / Manufacturer: Takeda Pharmaceuticals America, Inc.
Product type: PLASMA DERIVATIVE
Marketing category: Biologic License Application
Dosage form: INJECTION, SOLUTION
Routes: SUBCUTANEOUS
Marketing started: 20161018

FDA application: BLA125596

## Active ingredients

- HUMAN IMMUNOGLOBULIN G: 200 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0944-2850"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0944-2850