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Last Updated: November 24, 2024

ADVIL MIGRAINE LIQUI-GELS Drug Patent Profile


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When do Advil Migraine Liqui-gels patents expire, and what generic alternatives are available?

Advil Migraine Liqui-gels is a drug marketed by Haleon Us Holdings and is included in one NDA.

The generic ingredient in ADVIL MIGRAINE LIQUI-GELS is ibuprofen. There are sixty-four drug master file entries for this compound. Two hundred and thirty-eight suppliers are listed for this compound. Additional details are available on the ibuprofen profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Advil Migraine Liqui-gels

A generic version of ADVIL MIGRAINE LIQUI-GELS was approved as ibuprofen by STRIDES PHARMA on September 24th, 1986.

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Drug patent expirations by year for ADVIL MIGRAINE LIQUI-GELS
Recent Clinical Trials for ADVIL MIGRAINE LIQUI-GELS

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

SponsorPhase
Brigham and Women's HospitalPhase 4
VA Connecticut Healthcare SystemPhase 1
National Headache FoundationPhase 1

See all ADVIL MIGRAINE LIQUI-GELS clinical trials

Pharmacology for ADVIL MIGRAINE LIQUI-GELS

US Patents and Regulatory Information for ADVIL MIGRAINE LIQUI-GELS

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Haleon Us Holdings ADVIL MIGRAINE LIQUI-GELS ibuprofen CAPSULE;ORAL 020402-002 Mar 16, 2000 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

EU/EMA Drug Approvals for ADVIL MIGRAINE LIQUI-GELS

Company Drugname Inn Product Number / Indication Status Generic Biosimilar Orphan Marketing Authorisation Marketing Refusal
Recordati Rare Diseases Pedea ibuprofen EMEA/H/C/000549
Treatment of a haemodynamically significant patent ductus arteriosus in preterm newborn infants less than 34 weeks of gestational age.
Authorised no no no 2004-07-28
>Company >Drugname >Inn >Product Number / Indication >Status >Generic >Biosimilar >Orphan >Marketing Authorisation >Marketing Refusal

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