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Last Updated: April 18, 2024

Fexofenadine hydrochloride - Generic Drug Details


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What are the generic drug sources for fexofenadine hydrochloride and what is the scope of patent protection?

Fexofenadine hydrochloride is the generic ingredient in thirteen branded drugs marketed by Chattem Sanofi, Barr, P And L, Taro, Aurobindo Pharma Ltd, Dr Reddys Labs Ltd, Hetero Labs Ltd V, Rising, Sun Pharm Inds, Teva, Wockhardt, L Perrigo Co, Granules, Sciegen Pharms Inc, Unique, Aurobindo Pharma, Dr Reddys, Impax Pharms, and Sun Pharm, and is included in thirty-two NDAs. There is one patent protecting this compound and one Paragraph IV challenge. Additional information is available in the individual branded drug profile pages.

Fexofenadine hydrochloride has forty-three patent family members in thirty-eight countries.

There are twenty-one drug master file entries for fexofenadine hydrochloride. One hundred and one suppliers are listed for this compound. There are six tentative approvals for this compound.

Summary for fexofenadine hydrochloride
International Patents:43
US Patents:1
Tradenames:13
Applicants:19
NDAs:32
Drug Master File Entries: 21
Finished Product Suppliers / Packagers: 101
Raw Ingredient (Bulk) Api Vendors: 127
Clinical Trials: 78
Patent Applications: 2,629
Formulation / Manufacturing:see details
What excipients (inactive ingredients) are in fexofenadine hydrochloride?fexofenadine hydrochloride excipients list
DailyMed Link:fexofenadine hydrochloride at DailyMed
Recent Clinical Trials for fexofenadine hydrochloride

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

SponsorPhase
Dhaka Medical CollegePhase 2/Phase 3
Opella Healthcare Group SAS, a Sanofi CompanyPhase 3
Eurofarma Laboratorios S.A.Phase 3

See all fexofenadine hydrochloride clinical trials

Generic filers with tentative approvals for FEXOFENADINE HYDROCHLORIDE
Applicant Application No. Strength Dosage Form
⤷  Try a Trial⤷  Try a Trial60MG;120MGTABLET, EXTENDED RELEASE;ORAL
⤷  Try a Trial⤷  Try a Trial60/120MGTABLET, EXTENDED RELEASE; ORAL
⤷  Try a Trial⤷  Try a Trial180MGTABLET; ORAL

The 'tentative' approval signifies that the product meets all FDA standards for marketing, and, but for the patents / regulatory protections, it would approved.

Pharmacology for fexofenadine hydrochloride
Paragraph IV (Patent) Challenges for FEXOFENADINE HYDROCHLORIDE
Tradename Dosage Ingredient Strength NDA ANDAs Submitted Submissiondate
CHILDREN'S ALLEGRA HIVES Oral Suspension (OTC) fexofenadine hydrochloride 30 mg/5 mL 201373 1 2010-01-25

US Patents and Regulatory Information for fexofenadine hydrochloride

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
P And L CHILDREN'S FEXOFENADINE HYDROCHLORIDE HIVES fexofenadine hydrochloride SUSPENSION;ORAL 203330-002 Nov 18, 2014 OTC No Yes ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Dr Reddys Labs Ltd FEXOFENADINE HYDROCHLORIDE fexofenadine hydrochloride TABLET;ORAL 076502-003 Apr 11, 2006 AB RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Wockhardt FEXOFENADINE HYDROCHLORIDE ALLERGY fexofenadine hydrochloride TABLET;ORAL 079112-006 Feb 8, 2012 OTC No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
L Perrigo Co FEXOFENADINE HYDROCHLORIDE fexofenadine hydrochloride TABLET;ORAL 212971-002 Feb 24, 2020 OTC No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Teva FEXOFENADINE HYDROCHLORIDE fexofenadine hydrochloride TABLET;ORAL 076447-003 Sep 1, 2005 AB RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Rising CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGY fexofenadine hydrochloride TABLET;ORAL 077081-004 Jul 21, 2011 DISCN 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

Expired US Patents for fexofenadine hydrochloride

International Patents for fexofenadine hydrochloride

Country Patent Number Title Estimated Expiration
Russian Federation 2008128418 КОМПОЗИЦИЯ СУСПЕНЗИИ ФЕКСОФЕНАДИНА ⤷  Try a Trial
Slovenia 1965768 ⤷  Try a Trial
World Intellectual Property Organization (WIPO) 2007070517 ⤷  Try a Trial
Jordan 2549 مستحضر معلق فيكسوفينادين (Fexofenadine suspension formulation) ⤷  Try a Trial
New Zealand 568943 Fexofenadine suspension formulation ⤷  Try a Trial
Argentina 058323 FORMULACION DE SUSPENSION DE FEXOFENADINA ⤷  Try a Trial
>Country >Patent Number >Title >Estimated Expiration

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.