# Procainamide Hydrochloride

NDC: 14789-900
Generic name: Procainamide Hydrochloride
Labeler / Manufacturer: Nexus Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20071014

FDA application: ANDA206332

## Active ingredients

- PROCAINAMIDE HYDROCHLORIDE: 500 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"14789-900"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=14789-900
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d58751df-cd8b-45a6-8a32-af19e747e23a