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Last Updated: November 2, 2024

FOSFOMYCIN TROMETHAMINE Drug Patent Profile


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

Fosfomycin Tromethamine is a drug marketed by Alkem Labs Ltd, Amneal, Cipla, and Xiromed. and is included in four NDAs.

The generic ingredient in FOSFOMYCIN TROMETHAMINE is fosfomycin tromethamine. There are six drug master file entries for this compound. Six suppliers are listed for this compound. Additional details are available on the fosfomycin tromethamine profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Fosfomycin Tromethamine

A generic version of FOSFOMYCIN TROMETHAMINE was approved as fosfomycin tromethamine by XIROMED on October 6th, 2020.

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Summary for FOSFOMYCIN TROMETHAMINE
Drug patent expirations by year for FOSFOMYCIN TROMETHAMINE
Drug Prices for FOSFOMYCIN TROMETHAMINE

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Recent Clinical Trials for FOSFOMYCIN TROMETHAMINE

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SponsorPhase
Benova (Tianjin) Innovative medicine Research Co., Ltd.Phase 3
ZonMw: The Netherlands Organisation for Health Research and DevelopmentPhase 3
SaltroPhase 3

See all FOSFOMYCIN TROMETHAMINE clinical trials

Medical Subject Heading (MeSH) Categories for FOSFOMYCIN TROMETHAMINE

US Patents and Regulatory Information for FOSFOMYCIN TROMETHAMINE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Alkem Labs Ltd FOSFOMYCIN TROMETHAMINE fosfomycin tromethamine FOR SOLUTION;ORAL 214554-001 Oct 21, 2021 AA RX No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Xiromed FOSFOMYCIN TROMETHAMINE fosfomycin tromethamine FOR SOLUTION;ORAL 212548-001 Oct 6, 2020 AA RX No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Amneal FOSFOMYCIN TROMETHAMINE fosfomycin tromethamine FOR SOLUTION;ORAL 216600-001 Mar 25, 2024 AA RX No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Cipla FOSFOMYCIN TROMETHAMINE fosfomycin tromethamine FOR SOLUTION;ORAL 211881-001 Jan 26, 2022 AA 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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