# Ketamine Hydrochloride

NDC: 72572-321
Generic name: Ketamine Hydrochloride
Labeler / Manufacturer: Civica, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20191205

FDA application: ANDA074524

## Active ingredients

- KETAMINE HYDROCHLORIDE: 100 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72572-321"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72572-321
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=58c86d9b-8694-4bd8-8254-f19ee3ad60b0