51672-4170 : Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep Kit Oral Solution


NDC: 51672-4170
Labeler: Taro Pharmaceuticals U.S.a., Inc.
Product Type: Human Prescription Drug
Drug Name: Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep Kit
Dosage Form: Oral Solution
Application #: ANDA206431
Rev. Date: 


NDC Package Codes:

  • 51672-4170-5: 2 BOTTLE IN 1 CARTON (51672‑4170‑5) / 177 ML IN 1 BOTTLE

Active Ingredients:

  • Magnesium Sulfate
  • Unspecified Form
  • Potassium Sulfate
  • Sodium Sulfate Anhydrous

Dosage Strength:

  • 1.6 g/177mL
  • 3.13 g/177mL
  • 17.5 g/177mL

Pharmaceutical Classes:

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

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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.