NDC 63323-580
Atropine Sulfate 0.4 mg per 1 mL injection, 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 | Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action |
Product details
- Generic drug
- Atropine: every company that makes it
- Form
- injection, solution, endotracheal; intramedullary; intramuscular; intravenous; subcutaneous
- Strength
- 0.4 mg per 1 mL
- Approval
- NDA NDA209260
- On the market since
- Jan 23, 2017
- Package NDCs
63323-580-20- Official label
- DailyMed (National Library of Medicine), updated Oct 11, 2024
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