Last Updated: November 8, 2026

Cmp Dev Llc Company Profile

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What is the competitive landscape for CMP DEV LLC

CMP DEV LLC has seven approved drugs.

There are thirty-six US patents protecting CMP DEV LLC drugs.

Summary for Cmp Dev Llc
US Patents:36
Tradenames:7
Ingredients:7
NDAs:7

Drugs and US Patents for Cmp Dev Llc

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Cmp Dev Llc ATORVALIQ atorvastatin calcium SUSPENSION;ORAL 213260-001 Feb 1, 2023 RX Yes Yes 11,369,567 ⤷  Start Trial Y ⤷  Start Trial
Cmp Dev Llc QLONILIK clonidine hydrochloride SOLUTION;ORAL 221094-001 Jul 29, 2026 RX Yes Yes 12,551,466 ⤷  Start Trial Y ⤷  Start Trial
Cmp Dev Llc TADLIQ tadalafil SUSPENSION;ORAL 214522-001 Jun 17, 2022 RX Yes Yes 12,708,626 ⤷  Start Trial Y ⤷  Start Trial
Cmp Dev Llc NORLIQVA amlodipine besylate SOLUTION;ORAL 214439-001 Feb 24, 2022 RX Yes Yes 11,253,474 ⤷  Start Trial Y ⤷  Start Trial
Cmp Dev Llc TADLIQ tadalafil SUSPENSION;ORAL 214522-001 Jun 17, 2022 RX Yes Yes 12,691,120 ⤷  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

Supplementary Protection Certificates for Cmp Dev Llc Drugs

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
2059246 PA2024537 Lithuania ⤷  Start Trial PRODUCT NAME: (A) MACITENTANO ARBA JO FARMACINIU POZIURIU PRIIMTINOS DRUSKOS IR (B)TADALAFILIO ARBA JO FARMACINIU POZIURIU PRIIMTINOS DRUSKOS DERINYS; REGISTRATION NO/DATE: EU/1/24/1859 20240927
0740668 SPC/GB03/007 United Kingdom ⤷  Start Trial PRODUCT NAME: TADALAFIL AND PHARMACEUTICALLY ACCEPTABLE SALTS, ESTERS AND SOLVATES THEREOF.; REGISTERED: UK EU/1/02/237/001-004 20021114
1003503 05C0048 France ⤷  Start Trial PRODUCT NAME: AMLODIPINE OU UN DE SES SELS D?ADDITION D?ACIDES PHARMACAUTIQUEMENT ACCEPTABLES/ ATORVASTATINE OU UN DE SES SELS PHARMACEUTIQUEMENT ACCEPTABLES; REGISTRATION NO/DATE IN FRANCE: NL 29929 DU 20050707; REGISTRATION NO/DATE AT EEC: NL 29929 DU 20050707
0720599 122014000088 Germany ⤷  Start Trial PRODUCT NAME: EZETIMIB ODER PHARMAZEUTISCH ANNEHMBARE SALZE DAVON IN KOMBINATION MIT ATORVASTATIN ODER PHARMAZEUTISCH ANNEHMBARE SALZE DAVON, INSBESONDERE ATORVASTATIN ALS ATORVASTATINCALCIUMTRIHYDRAT; NAT. REGISTRATION NO/DATE: 90223.00.00 20141113; FIRST REGISTRATION: FRANKREICH CIS: 6 928 917 6 20140912
0443983 C300445 Netherlands ⤷  Start Trial PRODUCT NAME: VALSARTAN, AMLODIPINE EN HYDROCHLOORTHIAZIDE EN FARMACEUTISCH AANVAARDBARE ZOUTEN DAARVAN; REGISTRATION NO/DATE: EU/1/09/569/001-060 20091016
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description
Similar Applicant Names
Applicants may be listed under multiple names.
Here is a list of applicants with similar names.

Last updated: July 29, 2026

CMP DEV LLC Competitive Landscape Analysis: Market Position, Strengths & Strategic Insights

CMP DEV LLC’s competitive posture in branded and generic pharmaceutical development is defined by where its programs sit in the value chain: early R&D and CMC execution versus late-stage clinical/regulatory execution and monetization through licensing, settlements, or ANDA launches. The firm’s market impact is best evaluated by mapping (1) its pipeline stage and therapeutic focus, (2) whether it plays offense through Para IV filings or defense through exclusivity-protected commercialization, and (3) how its manufacturing and regulatory credibility affects customer or partner allocation decisions.

No complete, source-backed dataset is available in the prompt to identify CMP DEV LLC’s specific drug targets, portfolio companies, FDA submissions, Orange Book listings, Para IV litigation, settlements, registered facilities, or revenue/contract references. Under the operating constraints, producing an accurate competitive landscape with patent-expiration dates, litigation status, or product-level launch risk is not possible.

CMP DEV LLC market position

Featured snippet answer: Without verified program and regulatory identifiers, CMP DEV LLC’s market position cannot be quantified against specific competing drugs, competitors, or geographic commercialization.

What strengths does CMP DEV LLC bring to pharmaceutical development?

Featured snippet answer: Strengths depend on the firm’s actual portfolio execution (CMC performance, filing throughput, regulatory outcomes, and enforcement outcomes). No portfolio specifics are provided in the input.

Which competitive threats does CMP DEV LLC face in pharma?

Featured snippet answer: Competitive threats are typically defined by (1) faster generic challengers, (2) stronger CMC-ready competitors for difficult formulations, (3) patent estate durability of originators, and (4) customer preference for sponsors with established FDA track records. These require program-level mapping that is not present.

How does CMP DEV LLC compare with peers by stage and therapeutic focus?

Featured snippet answer: Stage and therapeutic focus comparisons require known pipeline candidates, indicated uses, dosage forms, and regulatory pathway details.

Which partnerships matter most to CMP DEV LLC’s growth strategy?

Featured snippet answer: Partnership strength is measurable only through documented collaboration agreements, sponsored filings, co-development sponsors, or license/supply agreements tied to specific assets.


Key Takeaways

  • CMP DEV LLC’s competitive landscape cannot be rendered with required patent, regulatory, litigation, or market-position specificity from the provided prompt.
  • A business-grade competitive analysis requires program-level identifiers (assets, sponsors, FDA submissions, and patent listings). Those are not supplied.

FAQs

  1. How do Para IV filing strategies typically change a developer’s competitive position?
  2. What metrics best compare CMC capability across generic developers?
  3. How should investors evaluate a sponsor’s likelihood of successful ANDA approval?
  4. What drives customer selection for co-development or licensing partnerships in pharma?
  5. How do patent estate strength and formulation complexity affect generic launch timing?

References

No sources were provided or extractable from the prompt.

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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.