# NALOXONE HYDROCHLORIDE

NDC: 50090-6963
Generic name: naloxone hydrochloride
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY
Routes: NASAL
Marketing started: 20230730

FDA application: ANDA211951

## 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:"50090-6963"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-6963
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=46f27d04-d4d2-4ef1-9cc5-4d58f4056f06