| NDC Code | 51662-1390-3 |
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| Package Description | 25 POUCH in 1 CASE (51662-1390-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1390-2) / 2 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 51662-1390 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Magnesium Sulfate |
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| Non-Proprietary Name | Magnesium Sulfate |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20191007 |
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| Marketing Category Name | NDA |
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| Application Number | NDA019316 |
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| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
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| Substance Name | MAGNESIUM SULFATE HEPTAHYDRATE |
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| Strength | 500 |
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| Strength Unit | mg/mL |
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| Pharmacy 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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