NDC 51662-1334
Procainamide Hci 100 mg per 1 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Hospira, Inc.'s NDC 0409-1902.
Where the pills inside were 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 |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
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
- Feb 10, 2019
- Package NDCs
51662-1334-151662-1334-251662-1334-3- Official label
- DailyMed (National Library of Medicine), updated Feb 19, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?