United States · FDA National Drug Code directory
Lutathera
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 69488-003_74d44dec-f079-43b7-94ac-989a948f53ec
- Product NDC
- 69488-003
- Form
- INJECTION
- Composition / generic term
- Lutetium Lu 177 dotatate
- Labeler
- Advanced Accelerator Applications USA, Inc
- Marketing category
- NDA
- Marketing start / end (source format)
- 20180126
- Source listing expiry
- 20271231
Source-listed ingredients
- LUTETIUM OXODOTREOTIDE LU-177 — 10 mCi/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 PACKAGE (69488-003-01) / 20.5 mL in 1 VIAL · 69488-003-01
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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