# Ketamine Hydrochloride

NDC: 25021-683
Generic name: Ketamine Hydrochloride
Labeler / Manufacturer: Sagent Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20230715

FDA application: ANDA216809

## 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:"25021-683"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=25021-683
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=902c3785-a3cb-472b-ac15-394ac646271d