Fluxid Patent Expiration

Fluxid is a drug owned by Ucb Inc. It is protected by 2 US drug patents filed in 2013 out of which all have expired. Based on its patents and exclusivities, its generic launch date is estimated to be Apr 09, 2018. Details of Fluxid's patents and their expiration are given in the table below.

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Drug Patent Number Drug Patent Title Drug Patent Expiry Status
These drug patents focus on the other aspects of the drug like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US6221392 Rapidly dissolving robust dosage form
Apr, 2018

(8 years ago)

Expired
US6024981 Rapidly dissolving robust dosage form
Apr, 2018

(8 years ago)

Expired

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US patents provide insights into the exclusivity only within the United States, but Fluxid is protected by patents in multiple countries. Understanding the full scope of patent protection is crucial in strategizing market entry. By looking at the broader patent landscape, you can identify markets with weaker patent protection which could be ideal generic entry points. The following section offers details on Fluxid's family patents as well as insights into ongoing legal events on those patents.

Fluxid's Family Patents


Family Patents

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Clinical Trials

Recent Clinical Trials on Fluxid:

Sometimes companies keep conducting clinical trials even after the drug's approval to discover new formulations, methods of use, or new treatment indications, so they could file for additional patents or receive regulatory exclusivity extensions, such as pediatric exclusivity, potentially delaying generic competition. Based on these recent clinical trials, generic companies need to consider the potential for new intellectual property or regulatory hurdles. These strategic moves by the drug owner might delay generic substitution or lead to additional sales of the brand drug, even after patent expiry.

Title Lead Sponsor Collaborators Status Phases
Clinical Trials
Antihistamines in the Treatment of Irritable Bowel Syndrome With Diarrhea University of Cincinnati NA WITHDRAWN
(Sep 1, 2026)
PHASE3
A Study to Learn How Different Preparations of Osivelotor Taste and Enter the Blood With Food or Liquids or With an Antacid in Healthy Adults Pfizer NA NOT YET RECRUITING
(Sep 1, 2026)
PHASE1
Study on the Effect of Famotidine on Pharmacokinetics of Taletrectinib Nuvation Bio Inc. NA NOT YET RECRUITING
(Jul 1, 2026)
PHASE1
Famotidine vs Placebo for the Treatment of Non-Hospitalized Adults With COVID-19 Northwell Health NA COMPLETED
(Jun 1, 2026)
PHASE2
A Phase 1, First-in-human Study of OKN4395 and Pembrolizumab in Patients With Solid Tumors Epkin NA RECRUITING
(Jun 1, 2026)
PHASE1
A Study to Assess the Effect of Famotidine on the Drug Levels of Afimetoran in Healthy Participants Bristol-Myers Squibb NA COMPLETED
(May 1, 2026)
PHASE1




Generic Launch

Generic Release Date:

Fluxid's generic launch date based on the expiry of its last outstanding patent is estimated to be Apr 09, 2018 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Fluxid Generic API suppliers:

Famotidine is the generic name for the brand Fluxid. 54 different companies have already filed for the generic of Fluxid, with Annora Pharma having the maximum number of approved applications. Check out the entire list of companies who have already received approval for Fluxid's generic

Alternative Brands for Fluxid

There are several other brand drugs using the same active ingredient (Famotidine) as Fluxid. Given below is the list of those companies and their brand drugs, to help you identify new opportunities, assess competitors, and plan your market strategies more effectively.

Drug Owner Drug Name
Horizon
Duexis
J And J Consumer Inc
Pepcid Ac
Kenvue Brands
Pepcid Ac
Pepcid Complete


Apart from brand drugs containing the same ingredient, some generics have also been filed for Famotidine, Fluxid's active ingredient. Check the complete list of approved generic manufacturers for Fluxid





About Fluxid

Fluxid is a drug owned by Ucb Inc. Fluxid uses Famotidine as an active ingredient. Fluxid was launched by Ucb in 2004.

Approval Date:

Fluxid was approved by FDA for market use on 24 September, 2004.

Active Ingredient:

Fluxid uses Famotidine as the active ingredient. Check out other Drugs and Companies using Famotidine ingredient

Dosage:

Fluxid is available in tablet, orally disintegrating form for oral use. Given below is detailed information on Dosage -

Strength Dosage Form Availability Application Pathway
20MG TABLET, ORALLY DISINTEGRATING Discontinued ORAL
40MG TABLET, ORALLY DISINTEGRATING Discontinued ORAL