# Vancomycin Hydrochloride

NDC: 71288-026
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: 20220727

FDA application: ANDA215196

## Active ingredients

- VANCOMYCIN HYDROCHLORIDE: 10 g/95mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71288-026"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-026
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=45642a47-4712-4a12-8cf7-ee6c2ab8e6c6