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Last Updated: June 23, 2024

SOLUPREP Drug Patent Profile


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Summary for SOLUPREP
US Patents:0
Applicants:1
NDAs:1
Formulation / Manufacturing:see details
DailyMed Link:SOLUPREP at DailyMed
Drug patent expirations by year for SOLUPREP
DrugPatentWatch® Estimated Loss of Exclusivity (LOE) Date for SOLUPREP
Generic Entry Date for SOLUPREP*:
Constraining patent/regulatory exclusivity:
REVISIONS TO THE LABELING TO DESCRIBE MODIFIED FORMULATION BASED ON RESULTS OF STUDIES EM-05-014624 AND EM-05-014815
NDA:
Dosage:
SOLUTION;TOPICAL

*The generic entry opportunity date is the latter of the last compound-claiming patent and the last regulatory exclusivity protection. Many factors can influence early or later generic entry. This date is provided as a rough estimate of generic entry potential and should not be used as an independent source.

Recent Clinical Trials for SOLUPREP

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

SponsorPhase
Fédération des médecins résidents du QuébecPhase 4
Centre for Interdisciplinary Research in Rehabilitation of Greater MontrealPhase 4
Claire BourgeoisPhase 4

See all SOLUPREP clinical trials

US Patents and Regulatory Information for SOLUPREP

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
3m Health Care SOLUPREP S chlorhexidine gluconate; isopropyl alcohol SOLUTION;TOPICAL 208288-001 Aug 8, 2018 OTC 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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