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Last Updated: April 23, 2024

SOJOURN Drug Patent Profile


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Which patents cover Sojourn, and what generic alternatives are available?

Sojourn is a drug marketed by Piramal Critical and is included in one NDA.

The generic ingredient in SOJOURN is sevoflurane. There are five drug master file entries for this compound. Nine suppliers are listed for this compound. Additional details are available on the sevoflurane profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Sojourn

A generic version of SOJOURN was approved as sevoflurane by BAXTER HLTHCARE on July 2nd, 2002.

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Drug patent expirations by year for SOJOURN
Recent Clinical Trials for SOJOURN

Identify potential brand extensions & 505(b)(2) entrants

SponsorPhase
Alberta Children's HospitalPhase 2
Emory UniversityPhase 4
Alberta Children's HospitalPhase 1

See all SOJOURN clinical trials

Pharmacology for SOJOURN
Drug ClassGeneral Anesthetic
Physiological EffectGeneral Anesthesia
Anatomical Therapeutic Chemical (ATC) Classes for SOJOURN

US Patents and Regulatory Information for SOJOURN

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Piramal Critical SOJOURN sevoflurane LIQUID;INHALATION 077867-001 May 2, 2007 AN RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

EU/EMA Drug Approvals for SOJOURN

Company Drugname Inn Product Number / Indication Status Generic Biosimilar Orphan Marketing Authorisation Marketing Refusal
Chanelle Pharmaceuticals Manufacturing Limited Sevohale (previously known as Sevocalm) sevoflurane EMEA/V/C/004199
For the induction and maintenance of anaesthesia.
Authorised yes no no 2016-06-21
Zoetis Belgium SA SevoFlo sevoflurane EMEA/V/C/000072
For the induction and maintenance of anaesthesia in dogs and cats.
Authorised no no no 2002-12-11
>Company >Drugname >Inn >Product Number / Indication >Status >Generic >Biosimilar >Orphan >Marketing Authorisation >Marketing Refusal

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