# Sodium Nitrite

NDC: 60267-311
Generic name: Sodium Nitrite
Labeler / Manufacturer: Hope Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20120214

FDA application: NDA203922

## Active ingredients

- SODIUM NITRITE: 30 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60267-311"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60267-311
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=52f01c6e-172a-47a9-98a6-9eab7651a032