# Bupivacaine hydrochloride

NDC: 70069-752
Generic name: Bupivacaine hydrochloride
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INFILTRATION, PERINEURAL
Marketing started: 20231127

FDA application: ANDA217792

## Active ingredients

- BUPIVACAINE HYDROCHLORIDE: 2.5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-752"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-752
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bcaab86f-20f0-4482-8d73-e29b36dced58