United States · FDA National Drug Code directory
NITHIODOTE
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 60267-812_74809468-0182-485a-bf62-e09489756a36
- Product NDC
- 60267-812
- Form
- KIT
- Composition / generic term
- Sodium Nitrite and Sodium Thiosulfate
- Labeler
- Hope Pharmaceuticals
- Marketing category
- NDA
- Marketing start / end (source format)
- 20110114
- Source listing expiry
- 20261231
Source-listed ingredients
Separate ingredient quantities are not available in this snapshot. Any composition term above is preserved as source text.
These values do not establish equivalence or a dose recommendation.
Packages
- 1 KIT in 1 CARTON (60267-812-00) * 10 mL in 1 VIAL, SINGLE-USE (60267-311-10) * 50 mL in 1 VIAL, SINGLE-DOSE (60267-705-50) · 60267-812-00
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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