# Gleostine

NDC: 24338-341
Generic name: lomustine
Labeler / Manufacturer: Azurity Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CAPSULE, GELATIN COATED
Routes: ORAL
Marketing started: 20251024

FDA application: NDA017588

## Active ingredients

- LOMUSTINE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24338-341"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24338-341
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3529fe2f-3c23-4862-bb20-b48026957082