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Procainamide Hydrochloride

NDC 14789-900 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerNexus Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA206332
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsPROCAINAMIDE HYDROCHLORIDE (500 mg/mL)
Marketing started20071014
Package count1

External sources

Source: openFDA. Public-domain (CC0).