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Potassium Phosphate

NDC 70069-747 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerSomerset Therapeutics, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA217726
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsDIBASIC POTASSIUM PHOSPHATE (236 mg/mL)
MONOBASIC POTASSIUM PHOSPHATE (224 mg/mL)
Marketing started20240711
Package count1

External sources

Source: openFDA. Public-domain (CC0).