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Magnesium Sulfate - 0517-2610-25 - (Magnesium Sulfate)

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Drug Information of Magnesium Sulfate

Product NDC: 0517-2610
Proprietary Name: Magnesium Sulfate
Non Proprietary Name: Magnesium Sulfate
Active Ingredient(s): 500    mg/mL & nbsp;   Magnesium Sulfate
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Magnesium Sulfate

Product NDC: 0517-2610
Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19900930

Package Information of Magnesium Sulfate

Package NDC: 0517-2610-25
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-2610-25) > 10 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Magnesium Sulfate

NDC Code 0517-2610-25
Proprietary Name Magnesium Sulfate
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-2610-25) > 10 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0517-2610
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Magnesium Sulfate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19900930
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name American Regent, Inc.
Substance Name MAGNESIUM SULFATE HEPTAHYDRATE
Strength Number 500
Strength Unit mg/mL
Pharmaceutical Classes Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA]

Complete Information of Magnesium Sulfate


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