NDC 60267-311

Sodium Nitrite 30 mg per 1 mL injection, solution

On the label: Hope Pharmaceuticals.

United States: 3

Where it's made

FactoryWhereRoleLast FDA inspection
Bora Pharmaceuticals Injectables Inc.Baltimore, MD, United StatesMakes it Problems found, fixed voluntarilyAug 10, 2023 · 12 inspections, 1 with FDA action
Pharmaceutics International, Inc.Cockeysville, MD, United StatesMakes it Serious problems, FDA actionMar 6, 2026 · 10 inspections, 2 with FDA action
Siegfried Grafton, Inc.Grafton, WI, United StatesMakes the active ingredient Problems found, fixed voluntarilyAug 21, 2026 · 7 inspections

Product details

Generic drug
Nitrite Ion: every company that makes it
Form
injection, solution, intravenous
Strength
30 mg per 1 mL
Approval
NDA NDA203922
On the market since
Feb 14, 2012
Package NDCs
60267-311-10
Official label
DailyMed (National Library of Medicine), updated Mar 9, 2026

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