# NALOXONE HYDROCHLORIDE

NDC: 68001-645
Generic name: naloxone hydrochloride
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY
Routes: NASAL
Marketing started: 20250501

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:"68001-645"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-645
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=327004b0-560a-84d0-e063-6294a90aa743