NDC 70518-4188
Atropine Sulfate 0.4 mg per 1 mL injection, solution
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Fresenius Kabi, LLC's NDC 63323-580.
Where the pills inside were 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
- Sep 26, 2024
- Package NDCs
70518-4188-070518-4188-1- Official label
- DailyMed (National Library of Medicine), updated Aug 31, 2026
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