# KETALAR

NDC: 0404-9880
Generic name: ketamine hydrochloride
Labeler / Manufacturer: Henry Schein, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20220111

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:"0404-9880"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0404-9880
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=46dab560-8ecd-4d92-8c92-6baa2310b09b