# Vancomycin Hydrochloride

NDC: 63323-284
Generic name: Vancomycin Hydrochloride
Labeler / Manufacturer: Fresenius Kabi, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20171026

FDA application: ANDA204107

## Active ingredients

- VANCOMYCIN HYDROCHLORIDE: 1 g/20mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-284"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-284
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=418c3c6a-d08d-448c-89c9-54e558c1ce16