52268-201 : Sutab Oral Tablet


NDC: 52268-201
Labeler: Braintree Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name:  Sutab
Dosage Form: Oral Tablet
Application #: NDA213135
Rev. Date: 


NDC Package Codes:

  • 52268-201-01: 2 BOTTLE, PLASTIC IN 1 KIT (52268‑201‑01) > 12 TABLET IN 1 BOTTLE, PLASTIC

Active Ingredients:

  • Sodium Sulfate
  • Magnesium Sulfate Anhydrous
  • Potassium Chloride

Dosage Strength:

  • 17.75 g/1
  • 2.7 g/1
  • 2.25 g/1

Pharmaceutical Classes:

  • Calculi Dissolution Agent [EPC]
  • Magnesium Ion Exchange Activity [MoA]
  • Osmotic Laxative [EPC]
  • Osmotic Activity [MoA]
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]
  • Increased Large Intestinal Motility [PE]
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
  • Potassium Compounds [CS]
  • Potassium Salt [EPC]

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.