# Acetazolamide

NDC: 23155-313
Generic name: Acetazolamide
Labeler / Manufacturer: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20211006

FDA application: ANDA202693

## Active ingredients

- ACETAZOLAMIDE SODIUM: 500 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"23155-313"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-313
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=60f656ff-97b1-4a89-99af-8100483c2bac