# Diazoxide

NDC: 13517-100
Generic name: diazoxide
Labeler / Manufacturer: e5 Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20191211

FDA application: ANDA211050

## 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:"13517-100"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=13517-100
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c0237320-2d3f-4907-a4d3-08f138aa4ca8