# Bupivacaine Hydrochloride

NDC: 73293-0002
Generic name: Bupivacaine hydrochloride
Labeler / Manufacturer: Huons Co., Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: SUBARACHNOID
Marketing started: 20191230

FDA application: ANDA212822

## Active ingredients

- BUPIVACAINE HYDROCHLORIDE: 7.5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"73293-0002"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=73293-0002
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2dc693df-3218-4a90-b3f7-21e80966a851