# Vancomycin Hydrochloride

NDC: 71288-022
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: 20220728

FDA application: ANDA215197

## Active ingredients

- VANCOMYCIN HYDROCHLORIDE: 500 mg/10mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71288-022"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-022
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=033efc76-11d5-4a93-91de-56ed41bab9c3