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Last Updated: November 21, 2024

MAGNESIUM Drug Patent Profile


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When do Magnesium patents expire, and when can generic versions of Magnesium launch?

Magnesium is a drug marketed by Santarus, B Braun Medical Inc, Exela Pharma, Fresenius Kabi Usa, Hospira, Baxter Hlthcare Corp, Hq Spclt Pharma, Mylan Labs Ltd, Amneal, Gland Pharma Ltd, and Milla Pharms. and is included in twenty NDAs.

The generic ingredient in MAGNESIUM is magnesium sulfate. There are one hundred and forty-six drug master file entries for this compound. Seventeen suppliers are listed for this compound. Additional details are available on the magnesium sulfate profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Magnesium

A generic version of MAGNESIUM was approved as magnesium sulfate by FRESENIUS KABI USA on September 8th, 1986.

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Drug patent expirations by year for MAGNESIUM
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Drug Sales Revenue Trends for MAGNESIUM

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US Patents and Regulatory Information for MAGNESIUM

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Hq Spclt Pharma MAGNESIUM SULFATE IN PLASTIC CONTAINER magnesium sulfate INJECTABLE;INJECTION 207350-005 Dec 6, 2017 AP RX No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Hospira MAGNESIUM SULFATE IN PLASTIC CONTAINER magnesium sulfate INJECTABLE;INJECTION 020309-003 Jan 26, 2007 AP RX Yes No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Mylan Labs Ltd MAGNESIUM SULFATE IN PLASTIC CONTAINER magnesium sulfate INJECTABLE;INJECTION 209911-001 Sep 14, 2018 AP RX No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Fresenius Kabi Usa MAGNESIUM SULFATE IN PLASTIC CONTAINER magnesium sulfate INJECTABLE;INJECTION 206485-005 Mar 15, 2016 AP RX No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Hospira MAGNESIUM SULFATE IN PLASTIC CONTAINER magnesium sulfate INJECTABLE;INJECTION 020309-001 Jun 24, 1994 AP RX Yes Yes ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Fresenius Kabi Usa MAGNESIUM SULFATE IN PLASTIC CONTAINER magnesium sulfate INJECTABLE;INJECTION 206485-002 Mar 15, 2016 AP RX No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

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