Last Updated: November 13, 2026

Merz Company Profile

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What is the competitive landscape for MERZ

MERZ has four approved drugs.

There are six US patents protecting MERZ drugs.

Summary for Merz
US Patents:6
Tradenames:4
Ingredients:4
NDAs:4
Patent Litigation for Merz: See patent lawsuits for Merz

Drugs and US Patents for Merz

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Merz Pharms ERYMAX erythromycin SOLUTION;TOPICAL 062508-002 Jul 11, 1985 DISCN No No ⤷  Start Trial ⤷  Start Trial
Merz INBRIJA levodopa POWDER;INHALATION 209184-001 Dec 21, 2018 RX Yes Yes 12,458,615 ⤷  Start Trial ⤷  Start Trial
Merz INBRIJA levodopa POWDER;INHALATION 209184-001 Dec 21, 2018 RX Yes Yes 8,945,612 ⤷  Start Trial Y ⤷  Start Trial
Merz INBRIJA levodopa POWDER;INHALATION 209184-001 Dec 21, 2018 RX Yes Yes 8,685,442 ⤷  Start Trial Y ⤷  Start 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 Merz

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Merz INBRIJA levodopa POWDER;INHALATION 209184-001 Dec 21, 2018 7,182,961 ⤷  Start Trial
Merz INBRIJA levodopa POWDER;INHALATION 209184-001 Dec 21, 2018 6,514,482 ⤷  Start Trial
Merz INBRIJA levodopa POWDER;INHALATION 209184-001 Dec 21, 2018 6,921,528 ⤷  Start Trial
Merz AMPYRA dalfampridine TABLET, EXTENDED RELEASE;ORAL 022250-001 Jan 22, 2010 8,663,685 ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration
Paragraph IV (Patent) Challenges for MERZ drugs
Drugname Dosage Strength Tradename Submissiondate
➤ Subscribe Extended-release Tablets 10 mg ➤ Subscribe 2014-01-22
➤ Subscribe Oral Solution 1 mg/5 mL ➤ Subscribe 2012-06-20

Supplementary Protection Certificates for Merz Drugs

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
3209302 202340008 Slovenia ⤷  Start Trial PRODUCT NAME: COMBINATION OF FOSLEVODOPA OR ITS PHARMACEUTICALLY ACCEPTABLE SALT AND FOSCARBIDOPA OR ITS PHARMACEUTICALLY ACCEPTABLE SALT; NATIONAL AUTHORISATION NUMBER: H/05/00514/002; DATE OF NATIONAL AUTHORISATION: 20221215; AUTHORITY FOR NATIONAL AUTHORISATION: SI; FIRST AUTHORISATION IN THE EUROPEAN ECONOMIC AREA: 141371; DATE OF FIRST AUTHORISATION IN THE EUROPEAN ECONOMIC AREA: 20220825; AUTHORITY OF FIRST AUTHORISATION IN THE EUROPEAN ECONOMIC AREA: AT
3209302 301224 Netherlands ⤷  Start Trial PRODUCT NAME: COMBINATIE VAN FOSLEVODOPA EN FOSCARBIDOPA, ELK DESGEWENST IN DE VORM VAN EEN FARMACEUTISCH AANVAARDBAAR ZOUT; NATIONAL REGISTRATION NO/DATE: RVG128752 20221107; FIRST REGISTRATION: AT 141371 20220826
3209302 CA 2023 00015 Denmark ⤷  Start Trial PRODUCT NAME: KOMBINATION AF FOSLEVODOPA ELLER ET FARMACEUTISK ACCEPTABELT SALT DERAF OG FOSCARBIDOPA ELLER ET FARMACEUTISK ACCEPTABELT SALT DERAF; NAT. REG. NO/DATE: 66549 (DK) 20221205; FIRST REG. NO/DATE: AT 141371 20220826
3209302 2023C/510 Belgium ⤷  Start Trial PRODUCT NAME: COMBINATIE VAN FOSLEVODOPA EN FOSCARBIDOPA, ELK IN ALLE VORMEN BESCHERMD DOOR HET BASISOCTROOI; AUTHORISATION NUMBER AND DATE: BE660571 20220901
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description
Similar Applicant Names
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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. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. 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.