# REXTOVY

NDC: 76329-3669
Generic name: Naloxone Hydrochloride
Labeler / Manufacturer: International Medication Systems, Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SPRAY
Routes: NASAL
Marketing started: 20240507

FDA application: NDA208969

## Active ingredients

- NALOXONE HYDROCHLORIDE: 4 mg/.25mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76329-3669"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76329-3669
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fe9735db-c57e-44a8-bffb-b87a84c2a6f3