40032-700 : Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate Oral Solution


NDC: 40032-700
Labeler: Novel Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name:  Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate
Dosage Form: Oral Solution
Application #: ANDA202511
Rev. Date: 


NDC Package Codes:

  • 40032-700-83: 2 BOTTLE IN 1 CARTON (40032‑700‑83) > 177 ML IN 1 BOTTLE

Active Ingredients:

  • Sodium Sulfate
  • Potassium Sulfate
  • Magnesium Sulfate Anhydrous

Dosage Strength:

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

Related Products:

Based on records with the same trade name.
  • 43386-700 Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate Oral Solution by Lupin Pharmaceuticals, 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.