NDC 63323-596
Glucagon 1 mg per 1 mL injection, powder, lyophilized, for solution
On the label: Fresenius Kabi, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Melrose Park, IL, United States | Makes it and tests it | Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action |
Product details
- Generic drug
- Glucagon: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intramuscular; intravenous
- Strength
- 1 mg per 1 mL
- Approval
- NDA NDA201849
- On the market since
- May 8, 2015
- Package NDCs
63323-596-0863323-596-16- Official label
- DailyMed (National Library of Medicine), updated Apr 1, 2022
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