# Dehydrated Alcohol

NDC: 82983-426
Generic name: Alcohol
Labeler / Manufacturer: Ajenat Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: PERCUTANEOUS
Marketing started: 20250815

FDA application: NDA207987

## Active ingredients

- ALCOHOL: 1 mL/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82983-426"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82983-426
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=636d6421-cadf-42b3-a431-ba40c06e36d2