NDC 0409-1902
Procainamide Hydrochloride 100 mg per 1 mL injection, solution
On the label: Hospira, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | Rocky Mount, NC, United States | Makes it, tests it, packages it and labels it | No problems foundFeb 7, 2025 · 11 inspections, 3 with FDA action |
Product details
- Generic drug
- Procainamide: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 100 mg per 1 mL
- Approval
- ANDA ANDA089069
- On the market since
- Mar 8, 2006
- Package NDCs
0409-1902-010409-1902-11- Official label
- DailyMed (National Library of Medicine), updated Jul 8, 2026
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