# Vancomycin Hydrochloride

NDC: 68001-407
Generic name: Vancomycin Hydrochloride
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20190823

FDA application: ANDA204125

## Active ingredients

- VANCOMYCIN HYDROCHLORIDE: 10 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-407"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-407
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f28e3c2b-ae31-4c2a-8178-53962b7b213c