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Last Updated: November 5, 2024

MICAFUNGIN IN SODIUM CHLORIDE 0.9% Drug Patent Profile


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Which patents cover Micafungin In Sodium Chloride 0.9%, and when can generic versions of Micafungin In Sodium Chloride 0.9% launch?

Micafungin In Sodium Chloride 0.9% is a drug marketed by Baxter Hlthcare Corp and is included in one NDA.

The generic ingredient in MICAFUNGIN IN SODIUM CHLORIDE 0.9% is micafungin sodium. There are eight drug master file entries for this compound. Thirteen suppliers are listed for this compound. Additional details are available on the micafungin sodium profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Micafungin In Sodium Chloride 0.9%

A generic version of MICAFUNGIN IN SODIUM CHLORIDE 0.9% was approved as micafungin sodium by FRESENIUS KABI USA on May 17th, 2019.

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Summary for MICAFUNGIN IN SODIUM CHLORIDE 0.9%
Drug patent expirations by year for MICAFUNGIN IN SODIUM CHLORIDE 0.9%
Recent Clinical Trials for MICAFUNGIN IN SODIUM CHLORIDE 0.9%

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SponsorPhase
Wake Forest University Health SciencesPhase 4
Scynexis, Inc.Phase 3
Yung Shin Pharm. Ind. Co., Ltd.Phase 4

See all MICAFUNGIN IN SODIUM CHLORIDE 0.9% clinical trials

Pharmacology for MICAFUNGIN IN SODIUM CHLORIDE 0.9%

US Patents and Regulatory Information for MICAFUNGIN IN SODIUM CHLORIDE 0.9%

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Baxter Hlthcare Corp MICAFUNGIN IN SODIUM CHLORIDE 0.9% micafungin sodium SOLUTION;INTRAVENOUS 216142-001 Sep 29, 2023 RX Yes Yes ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Baxter Hlthcare Corp MICAFUNGIN IN SODIUM CHLORIDE 0.9% micafungin sodium SOLUTION;INTRAVENOUS 216142-002 Sep 29, 2023 RX Yes Yes ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Baxter Hlthcare Corp MICAFUNGIN IN SODIUM CHLORIDE 0.9% micafungin sodium SOLUTION;INTRAVENOUS 216142-003 Sep 29, 2023 RX Yes Yes ⤷  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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