# KETAMINE HYDROCHLORIDE

NDC: 43066-177
Generic name: KETAMINE HYDROCHLORIDE
Labeler / Manufacturer: Baxter Healthcare Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20250917

FDA application: ANDA219684

## 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:"43066-177"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43066-177
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=549d6ed3-3c9b-4ea2-8aaf-f61d43e04602