# Ketalar

NDC: 42023-113
Generic name: ketamine hydrochloride
Labeler / Manufacturer: Par Health USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20071001

FDA application: NDA016812

## Active ingredients

- KETAMINE HYDROCHLORIDE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42023-113"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42023-113
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=14e8f864-8b8a-4e7e-8439-e510d3107063