| NDC Code | 51672-4170-5 |
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| Package Description | 2 BOTTLE in 1 CARTON (51672-4170-5) / 177 mL in 1 BOTTLE |
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| Product NDC | 51672-4170 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Sodium Sulfate, Potassium Sulfate, And Magnesium Sulfate Bowel Prep Kit |
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| Non-Proprietary Name | Sodium Sulfate Anhydrous, Potassium Sulfate, And Magnesium Sulfate |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20240327 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA206431 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | MAGNESIUM SULFATE, UNSPECIFIED FORM; POTASSIUM SULFATE; SODIUM SULFATE ANHYDROUS |
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| Strength | 1.6; 3.13; 17.5 |
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| Strength Unit | g/177mL; g/177mL; g/177mL |
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| Pharmacy Classes | Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |
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