# Diazoxide

NDC: 0254-1010
Generic name: Diazoxide
Labeler / Manufacturer: Par Health USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20200721

FDA application: ANDA210799

## Active ingredients

- DIAZOXIDE: 50 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0254-1010"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0254-1010
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=abe317a5-6c63-469c-89c8-9fedfe859c3d