# Vancomycin Hydrochloride

NDC: 87188-202
Generic name: Vancomycin Hydrochloride
Labeler / Manufacturer: Plano Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20100427

FDA application: ANDA090250

## Active ingredients

- VANCOMYCIN HYDROCHLORIDE: 1 g/20mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"87188-202"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=87188-202
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4983e3c8-e0f2-b366-e063-6394a90a9557