Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit 1.6 g/177mL
sodium sulfate anhydrous, potassium sulfate, and magnesium sulfate · SOLUTION · Sun Pharmaceutical Industries, Inc.
Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit is a solution containing sodium sulfate anhydrous, potassium sulfate, and magnesium sulfate at 1.6 g/177mL, taken oral. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit
- Generic Name
- sodium sulfate anhydrous, potassium sulfate, and magnesium sulfate
- NDC Code (Product)
51672-4170- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- 1.6 g/177mL
- Dosage Form
- SOLUTION
- Route
- ORAL
- Marketing Status
- Application #
- ANDA206431
- Marketing Start
- 03/27/2024
Recall History
No Recall HistoryFrequently Asked Questions
What is Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit used for?
Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit contains sodium sulfate anhydrous, potassium sulfate, and magnesium sulfate. It is a solution taken oral. Consult your doctor for specific uses.
Is Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit a controlled substance?
Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit is not classified as a controlled substance by the DEA.
What is the generic name for Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit?
The generic name for Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit is sodium sulfate anhydrous, potassium sulfate, and magnesium sulfate. There are no other listed brand versions of sodium sulfate anhydrous, potassium sulfate, and magnesium sulfate.
What is the NDC code for Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit 1.6 g/177mL?
The NDC (National Drug Code) for Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit 1.6 g/177mL is 51672-4170, listed by Sun Pharmaceutical Industries, Inc..
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
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