# Acetazolamide

NDC: 39822-0190
Generic name: Acetazolamide
Labeler / Manufacturer: XGen Pharmaceuticals DJB, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20081210

FDA application: ANDA040784

## Active ingredients

- ACETAZOLAMIDE SODIUM: 500 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"39822-0190"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=39822-0190
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a9199d3c-ce52-4db5-aa36-408f4e15e344