# Goprelto

NDC: 70839-359
Generic name: cocaine hydrochloride
Labeler / Manufacturer: LXO US Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION
Routes: NASAL
Marketing started: 20240209

FDA application: NDA209963

## Active ingredients

- COCAINE HYDROCHLORIDE: 40 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70839-359"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70839-359
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0f897764-fe30-090a-e063-6294a90af106