# Lutathera

NDC: 69488-003
Generic name: Lutetium Lu 177 dotatate
Labeler / Manufacturer: Advanced Accelerator Applications USA, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20180126

FDA application: NDA208700

## Active ingredients

- LUTETIUM OXODOTREOTIDE LU-177: 10 mCi/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69488-003"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69488-003
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=72d1a024-00b7-418a-b36e-b2cb48f2ab55