NDC 70710-2164
Ascorbic acid 500 mg per 1 mL injection
On the label: Zydus Pharmaceuticals (USA) Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Vadodara, India | Makes it and tests it | Serious problems, FDA actionApr 23, 2024 · 2 inspections, 1 with FDA action |
Product details
- Generic drug
- Ascorbic Acid: every company that makes it
- Form
- injection, intravenous
- Strength
- 500 mg per 1 mL
- Approval
- ANDA ANDA220873
- On the market since
- Sep 28, 2026
- Package NDCs
70710-2164-870710-2164-9- Official label
- DailyMed (National Library of Medicine), updated Sep 3, 2026
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