# DIURIL

NDC: 65649-311
Generic name: CHLOROTHIAZIDE
Labeler / Manufacturer: Salix Pharmaceuticals, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 19620215
Marketing ended: 20280131
FDA application: NDA011870

## Active ingredients

- CHLOROTHIAZIDE: 250 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65649-311"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65649-311
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bd936e35-1af8-42da-bcc0-f22489d68574