| NDC Code | 72603-278-02 |
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| Package Description | 2 BOTTLE, PLASTIC in 1 CARTON (72603-278-02) / 177 mL in 1 BOTTLE, PLASTIC (72603-278-01) |
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| Product NDC | 72603-278 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Sodium Sulfate, Potassium Sulfate And Magnesium Sulfate |
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| Non-Proprietary Name | Sodium Sulfate, 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 | 20250301 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212903 |
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| Manufacturer | NorthStar RxLLC |
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| Substance Name | MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE |
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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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