# Potassium Phosphate

NDC: 70069-747
Generic name: Potassium Phosphate
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20240711

FDA application: ANDA217726

## Active ingredients

- DIBASIC POTASSIUM PHOSPHATE: 236 mg/mL
- MONOBASIC POTASSIUM PHOSPHATE: 224 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-747"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-747
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=52f07402-1869-4a97-9c92-9729dc611f85