# KETAMINE HYDROCHLORIDE

NDC: 0404-9882
Generic name: ketamine hydrochloride
Labeler / Manufacturer: Henry Schein, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20220111

FDA application: ANDA074549

## Active ingredients

- KETAMINE HYDROCHLORIDE: 50 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0404-9882"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0404-9882
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dd8eff00-b92e-4f48-8b57-0464484d6ddf