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Serving leading biopharmaceutical companies globally:

Merck
Novartis
AstraZeneca
Dow
Federal Trade Commission
Chinese Patent Office
Johnson and Johnson
UBS
Cantor Fitzgerald
Accenture

Generated: February 23, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 202411

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NDA 202411 describes MAGNESIUM SULFATE, which is a drug marketed by Exela Pharma Scs Llc, Fresenius Kabi Usa, Hospira, Hospira Inc, and Hq Spclt Pharma, and is included in ten NDAs. It is available from eight suppliers. Additional details are available on the MAGNESIUM SULFATE profile page.

The generic ingredient in MAGNESIUM SULFATE is magnesium sulfate. There are one hundred and thirty-seven drug master file entries for this compound. Ten suppliers are listed for this compound. Additional details are available on the magnesium sulfate profile page.
Summary for 202411
Tradename:MAGNESIUM SULFATE
Applicant:Hospira Inc
Ingredient:magnesium sulfate
Patents:0
Therapeutic Class:Therapeutic Nutrients/Minerals/Electrolytes
Formulation / Manufacturing:see details
Suppliers and Packaging for NDA: 202411
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
MAGNESIUM SULFATE magnesium sulfate SOLUTION;INTRAMUSCULAR, INTRAVENOUS 202411 ANDA Hospira, Inc. 0409-2168 N 0409-2168-02

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:SOLUTION;INTRAMUSCULAR, INTRAVENOUSStrength10GM/20ML (500MG/ML)
Approval Date:May 14, 2015TE:RLD:No

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US Department of Justice
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