# ketamine hydrochloride

NDC: 65219-188
Generic name: ketamine hydrochloride
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20230710

FDA application: ANDA215808

## 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:"65219-188"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-188
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cc67b0fd-ca73-49f6-b5ca-705dc7331776