# Acetazolamide

NDC: 67457-853
Generic name: acetazolamide sodium
Labeler / Manufacturer: Mylan Institutional LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20180913

FDA application: ANDA200880

## Active ingredients

- ACETAZOLAMIDE SODIUM: 500 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67457-853"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67457-853
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=521838b0-a10d-495f-a014-f9ff25a6b6f3