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Magnesium Sulfate - 0409-6730-13 - (MAGNESIUM SULFATE HEPTAHYDRATE)

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Drug Information of Magnesium Sulfate

Product NDC: 0409-6730
Proprietary Name: Magnesium Sulfate
Non Proprietary Name: MAGNESIUM SULFATE HEPTAHYDRATE
Active Ingredient(s): 4    g/50mL & nbsp;   MAGNESIUM SULFATE HEPTAHYDRATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Magnesium Sulfate

Product NDC: 0409-6730
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020309
Marketing Category: NDA
Start Marketing Date: 19940624

Package Information of Magnesium Sulfate

Package NDC: 0409-6730-13
Package Description: 24 POUCH in 1 CASE (0409-6730-13) > 1 BAG in 1 POUCH > 50 mL in 1 BAG

NDC Information of Magnesium Sulfate

NDC Code 0409-6730-13
Proprietary Name Magnesium Sulfate
Package Description 24 POUCH in 1 CASE (0409-6730-13) > 1 BAG in 1 POUCH > 50 mL in 1 BAG
Product NDC 0409-6730
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MAGNESIUM SULFATE HEPTAHYDRATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19940624
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name MAGNESIUM SULFATE HEPTAHYDRATE
Strength Number 4
Strength Unit g/50mL
Pharmaceutical Classes Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA]

Complete Information of Magnesium Sulfate


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