NDC 40032-700

SODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATE

Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate

SODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATE is a Oral Solution in the Human Prescription Drug category. It is labeled and distributed by Novel Laboratories, Inc.. The primary component is Sodium Sulfate; Potassium Sulfate; Magnesium Sulfate Anhydrous.

Product ID40032-700_dc9d6a79-3160-4122-a0d7-139148afe782
NDC40032-700
Product TypeHuman Prescription Drug
Proprietary NameSODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATE
Generic NameSodium Sulfate, Potassium Sulfate, Magnesium Sulfate
Dosage FormSolution
Route of AdministrationORAL
Marketing Start Date2017-02-23
Marketing CategoryANDA / ANDA
Application NumberANDA202511
Labeler NameNovel Laboratories, Inc.
Substance NameSODIUM SULFATE; POTASSIUM SULFATE; MAGNESIUM SULFATE ANHYDROUS
Active Ingredient Strength18 g/177mL; g/177mL; g/177mL
Pharm ClassesOsmotic 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],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]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 40032-700-83

2 BOTTLE in 1 CARTON (40032-700-83) > 177 mL in 1 BOTTLE
Marketing Start Date2017-02-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 40032-700-83 [40032070083]

SODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATE SOLUTION
Marketing CategoryANDA
Application NumberANDA202511
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-02-23

Drug Details

Active Ingredients

IngredientStrength
SODIUM SULFATE17.5 g/177mL

OpenFDA Data

SPL SET ID:af53cca9-d7db-4723-ad7a-bee09484dbb0
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1120068
  • 1001689
  • Pharmacological Class

    • 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]
    • 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]
    • 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]
    • 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]

    NDC Crossover Matching brand name "SODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATE" or generic name "Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate"

    NDCBrand NameGeneric Name
    40032-700SODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATEsodium sulfate, potassium sulfate, magnesium sulfate
    43386-700SODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATEsodium sulfate, potassium sulfate, magnesium sulfate
    10572-012SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATEsodium sulfate, potassium sulfate, magnesium sulfate
    10572-112SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATEsodium sulfate, potassium sulfate, magnesium sulfate
    52268-012SUPREP Bowel Prepsodium sulfate, potassium sulfate, magnesium sulfate
    52268-112SUPREP Bowel Prepsodium sulfate, potassium sulfate, magnesium sulfate

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