# Acetazolamide

NDC: 50742-233
Generic name: Acetazolamide
Labeler / Manufacturer: Ingenus Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20170731

FDA application: ANDA203434

## Active ingredients

- ACETAZOLAMIDE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50742-233"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50742-233
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a1f6ed35-9188-4115-8a3c-1ac91c07bf7d