# VANCOMYCIN HYDROCHLORIDE

NDC: 31722-210
Generic name: VANCOMYCIN HYDROCHLORIDE
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220706

FDA application: ANDA216591

## 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:"31722-210"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-210
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3f5dacea-af40-4103-b128-c5e0c0c52fa1