NDC 0404-9784
Atropine Sulfate 0.1 mg per 1 mL injection, solution
On the label: Henry Schein, Inc.. It's repackaged: Henry Schein, Inc. rebottles it from Amneal Pharmaceuticals LLC's NDC 70121-1705.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Amneal Pharmaceuticals Private Limited | Ahmedabad, India | Makes it, tests it, packages it and sterilizes it | No problems foundJun 19, 2024 · 7 inspections |
Product details
- Generic drug
- Atropine: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 0.1 mg per 1 mL
- Approval
- ANDA ANDA215342
- On the market since
- Jun 16, 2025
- Package NDCs
0404-9784-05- Official label
- DailyMed (National Library of Medicine), updated Jul 28, 2026
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