# Naloxone Hydrochloride

NDC: 0480-3478
Generic name: Naloxone Hydrochloride
Labeler / Manufacturer: Teva Pharmaceuticals, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY, METERED
Routes: NASAL
Marketing started: 20240923

FDA application: ANDA209522

## Active ingredients

- NALOXONE HYDROCHLORIDE: 4 mg/.1mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0480-3478"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0480-3478
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3a73ee4b-c2a4-496f-be90-9f78c8046062