# NITHIODOTE

NDC: 60267-812
Generic name: Sodium Nitrite and Sodium Thiosulfate
Labeler / Manufacturer: Hope Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: KIT
Routes: —
Marketing started: 20110114

FDA application: NDA201444

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60267-812"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60267-812
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ff4941b3-9901-4aab-adcf-c5327bede34e