SUTAB 2.7 g/1
sodium sulfate, magnesium sulfate, and potassium chloride · TABLET · Braintree Laboratories, Inc.
SUTAB is a tablet containing sodium sulfate, magnesium sulfate, and potassium chloride at 2.7 g/1, taken oral. Manufactured by Braintree Laboratories, Inc..
Key Facts
- Brand Name
- SUTAB
- Generic Name
- sodium sulfate, magnesium sulfate, and potassium chloride
- NDC Code (Product)
52268-201- Manufacturer
- Braintree Laboratories, Inc.
- Strength
- 2.7 g/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- NDA213135
- Marketing Start
- 11/10/2020
Recall History
No Recall HistoryFrequently Asked Questions
What is SUTAB used for?
SUTAB contains sodium sulfate, magnesium sulfate, and potassium chloride. It is a tablet taken oral. Consult your doctor for specific uses.
Is SUTAB a controlled substance?
SUTAB is not classified as a controlled substance by the DEA.
What is the generic name for SUTAB?
The generic name for SUTAB is sodium sulfate, magnesium sulfate, and potassium chloride. There are no other listed brand versions of sodium sulfate, magnesium sulfate, and potassium chloride.
What is the NDC code for SUTAB 2.7 g/1?
The NDC (National Drug Code) for SUTAB 2.7 g/1 is 52268-201, listed by Braintree Laboratories, Inc..
Other SUTAB Dosages
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)