# Vancomycin hydrochloride

NDC: 71288-024
Generic name: Vancomycin hydrochloride
Labeler / Manufacturer: Meitheal Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220915

FDA application: ANDA215195

## Active ingredients

- VANCOMYCIN HYDROCHLORIDE: 750 mg/15mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71288-024"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-024
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e5e26614-4119-40cc-b092-48ab97a41287