# Vancomycin Hydrochloride

NDC: 63323-314
Generic name: VANCOMYCIN HYDROCHLORIDE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20041130

FDA application: ANDA062663

## Active ingredients

- VANCOMYCIN HYDROCHLORIDE: 10 g/100mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-314"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-314
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0713a847-a334-4b73-af22-343aa06621b9