# Naloxone Hydrochloride

NDC: 51316-210
Generic name: Naloxone Hydrochloride
Labeler / Manufacturer: CVS Pharmacy, Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY
Routes: NASAL
Marketing started: 20240424

FDA application: ANDA217992

## 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:"51316-210"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51316-210
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=840e017d-0142-4d0e-a80e-327ac44bc0c5