Levemir Penfill Patent Expiration

Levemir Penfill is a drug owned by Novo Nordisk Inc. It is protected by 4 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 Jun 16, 2019. Details of Levemir Penfill's patents and their expiration are given in the table below.

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).
US5750497 Acylated insulin
Jun, 2019

(5 years ago)

Expired
US5866538 Insulin preparations containing NaCl
Jun, 2017

(7 years ago)

Expired
US6011007 Acylated insulin
Feb, 2014

(10 years ago)

Expired
US6869930 Acylated insulin
Feb, 2014

(10 years ago)

Expired

Stay ahead of others in designing the generic launch strategy of these 5 blockbuster drugs expiring in next 5 years.

Get the exclusive patent insights now. Don't be the last to know.

US patents provide insights into the exclusivity only within the United States, but Levemir Penfill 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 Levemir Penfill's family patents as well as insights into ongoing legal events on those patents.

Levemir Penfill's Family Patents


Family Patents

Explore Our Curated Drug Screens

Drugs Generating Over $1 Billion in Annual Revenue
Explore the top-performing drugs that dominate the pharmaceutical industry
View List
NCE-1 Patent Expiry in the Next 1 Year
Identify opportunities as new chemical entity (NCE-1) patents approach expiry
View List
Recently Granted Patents in EP
Find the opportunity to file Oppositions
View List


Generic Launch

Generic Release Date:

Levemir Penfill's generic launch date based on the expiry of its last outstanding patent is estimated to be Jun 16, 2019 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Levemir Penfill Generics:

There are no approved generic versions for Levemir Penfill as of now.

Alternative Brands for Levemir Penfill

Levemir Penfill which is used for managing blood sugar levels in patients with diabetes mellitus., has several other brand drugs in the same treatment category and using the same active ingredient (Insulin Detemir Recombinant). 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 Treatment Area
Novo Nordisk Inc
Levemir

(uses Insulin Detemir Recombinant)

Used for managing diabetes mellitus by providing long-acting basal insulin.
Levemir Flexpen

(uses Insulin Detemir Recombinant)

Used for managing blood sugar levels in patients with diabetes mellitus.
Levemir Innolet

(uses Insulin Detemir Recombinant)

Used for managing blood sugar levels in patients with diabetes mellitus.
Levemir Flextouch

(uses Insulin Detemir Recombinant)

Used for managing blood sugar levels in patients with diabetes mellitus.





About Levemir Penfill

Levemir Penfill is a drug owned by Novo Nordisk Inc. It is used for managing blood sugar levels in patients with diabetes mellitus. Levemir Penfill uses Insulin Detemir Recombinant as an active ingredient. Levemir Penfill was launched by Novo Nordisk Inc in 2013.

Approval Date:

Levemir Penfill was approved by FDA for market use on 31 October, 2013.

Active Ingredient:

Levemir Penfill uses Insulin Detemir Recombinant as the active ingredient. Check out other Drugs and Companies using Insulin Detemir Recombinant ingredient

Treatment:

Levemir Penfill is used for managing blood sugar levels in patients with diabetes mellitus.

Dosage:

Levemir Penfill is available in injectable form for subcutaneous use. Given below is detailed information on Dosage -

Strength Dosage Form Availability Application Pathway
300 UNITS/3ML (100 UNITS/ML) INJECTABLE Discontinued SUBCUTANEOUS