52268-012 : Suprep Bowel Prep Oral Solution, Concentrate


NDC: 52268-012
Labeler: Braintree Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name:  Suprep Bowel Prep
Dosage Form: Oral Solution, Concentrate
Application #: NDA022372
Rev. Date: 


NDC Package Codes:

  • 52268-012-01: 2 BOTTLE, PLASTIC IN 1 CARTON (52268‑012‑01) > 177.4 ML IN 1 BOTTLE, PLASTIC

Active Ingredients:

  • Magnesium Sulfate
  • Potassium Sulfate
  • Sodium Sulfate

Dosage Strength:

  • 1.6 g/mL
  • 3.13 g/mL
  • 17.5 g/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 52268-112 Suprep Bowel Prep Oral Solution, Concentrate by Braintree Laboratories, Inc.

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.