# Vancomycin Hydrochloride

NDC: 68462-955
Generic name: Vancomycin Hydrochloride
Labeler / Manufacturer: GLENMARK PHARMACEUTICALS INC., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20260412

FDA application: ANDA205694

## 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:"68462-955"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-955
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=74056e26-57fd-448e-af76-edbccfc3efb7