# E-Z-HD

NDC: 32909-764
Generic name: barium sulfate
Labeler / Manufacturer: E-Z-EM Canada Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20160111

FDA application: NDA208036

## Active ingredients

- BARIUM SULFATE: 980 mg/g

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"32909-764"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=32909-764
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a4330804-7179-472a-91cb-84bbd5079bb8