NDC 70518-3120
Atropine Sulfate 0.1 mg per 1 mL injection
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from International Medication Systems, Ltd.'s NDC 76329-3340.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| International Medication Systems, Ltd. | South El Monte, CA, United States | Makes it, makes the active ingredient and tests it | Serious problems, FDA actionDec 19, 2025 · 15 inspections, 1 with FDA action |
Product details
- Generic drug
- Atropine: every company that makes it
- Form
- injection, intravenous
- Strength
- 0.1 mg per 1 mL
- Approval
- ANDA ANDA212461
- On the market since
- Jun 14, 2021
- Package NDCs
70518-3120-0- Official label
- DailyMed (National Library of Medicine), updated Apr 3, 2026
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