NDC 65219-801
Glycopyrrolate 0.2 mg per 1 mL injection, solution
On the label: Fresenius Kabi USA, 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
- Glycopyrronium: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 0.2 mg per 1 mL
- Approval
- ANDA ANDA209328
- On the market since
- Dec 31, 2023
- Package NDCs
65219-801-0065219-801-01- Official label
- DailyMed (National Library of Medicine), updated Sep 22, 2023
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