# SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE

NDC: 52536-175
Generic name: sodium sulfate, potassium sulfate, magnesium sulfate
Labeler / Manufacturer: Wilshire Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION, CONCENTRATE
Routes: ORAL
Marketing started: 20260415

FDA application: NDA022372

## Active ingredients

- MAGNESIUM SULFATE, UNSPECIFIED FORM: 1.6 g/mL
- POTASSIUM SULFATE: 3.13 g/mL
- SODIUM SULFATE: 17.5 g/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"52536-175"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=52536-175
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f269929e-c2ff-4288-9d3b-7770bcb5a498