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Magnesium Sulfate - 63323-064-20 - (MAGNESIUM SULFATE HEPTAHYDRATE)

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Drug Information of Magnesium Sulfate

Product NDC: 63323-064
Proprietary Name: Magnesium Sulfate
Non Proprietary Name: MAGNESIUM SULFATE HEPTAHYDRATE
Active Ingredient(s): 500    mg/mL & nbsp;   MAGNESIUM SULFATE HEPTAHYDRATE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Magnesium Sulfate

Product NDC: 63323-064
Labeler Name: Fresenius Kabi USA, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019316
Marketing Category: NDA
Start Marketing Date: 20000808

Package Information of Magnesium Sulfate

Package NDC: 63323-064-20
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-064-20) > 20 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Magnesium Sulfate

NDC Code 63323-064-20
Proprietary Name Magnesium Sulfate
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-064-20) > 20 mL in 1 VIAL, SINGLE-DOSE
Product NDC 63323-064
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MAGNESIUM SULFATE HEPTAHYDRATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20000808
Marketing Category Name NDA
Labeler Name Fresenius Kabi USA, LLC
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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