NDC 14789-900
Procainamide Hydrochloride 500 mg per 1 mL injection
On the label: Nexus Pharamaceuticals Inc..
Where it's made
This label doesn't name the factory that makes the drug (it lists 1 site that tests 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 Nexus Pharamaceuticals Inc. names for other drugs.
Product details
- Generic drug
- Procainamide: every company that makes it
- Form
- injection, intramuscular; intravenous
- Strength
- 500 mg per 1 mL
- Approval
- ANDA ANDA206332
- On the market since
- Oct 14, 2007
- Package NDCs
14789-900-02- Official label
- DailyMed (National Library of Medicine), updated Dec 2, 2025
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