NDC 51662-1392
Procainamide Hci 500 mg per 1 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged from NDC 0409-1903, made by Hospira, Inc. (Procainamide Hydrochloride). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that relabels it). Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants HF Acquisition Co. LLC. DBA HealthFirst names for other drugs.
Product details
- Generic drug
- Procainamide: every company that makes it
- Form
- injection, solution
- Strength
- 500 mg per 1 mL
- Approval
- ANDA ANDA089070
- On the market since
- Oct 16, 2019
- Package NDCs
51662-1392-151662-1392-251662-1392-3- Official label
- DailyMed (National Library of Medicine), updated Apr 24, 2023
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