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Pharmaceutical manufacturers of Sitagliptin

Find trusted suppliers of Sitagliptin. Explore verified pharmaceutical manufacturers worldwide for your sourcing needs.

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80results for pharmaceutical manufacturers of Sitagliptin

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  • Small logo of Teva Pharmaceutical Industries

    Teva Pharmaceutical Industries

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IsraelIsrael

    Sites

    Flag of IndiaIndia
    Flag of SpainSpain
    Flag of NetherlandsNetherlands
    Flag of PolandPoland
    Flag of Czech RepublicCzech Republic
    Flag of IsraelIsrael
    Flag of HungaryHungary
    Flag of ItalyItaly
    Flag of CroatiaCroatia
    Flag of MaltaMalta
    Flag of People's Republic of ChinaPeople's Republic of China
    Flag of Puerto RicoPuerto Rico
    Flag of MexicoMexico
    Flag of United States of AmericaUnited States of America
    Flag of GermanyGermany
    Flag of LithuaniaLithuania
    Flag of United KingdomUnited Kingdom
    Flag of IrelandIreland
    Flag of CanadaCanada

    Regulatory compliance

    EDQM
    WHO GMP
    FDA
    JDMF
    KDMF
    GDUFA
    EU WC
    GDP
    USDMF
    NDC API
    CEP COS

    Audit standards

    GMP (Finished Dosage)
    Sterile FDF
    GMP (APIs)

    Company description

    TAPI stands as the primary global provider of active pharmaceutical ingredients (APIs). With the most extensive range of over 370 high-caliber API products in the industry, we cater to almost 1,000 clients across more than 100 nations. Operating as an independent division under Teva Pharmaceutical Industries, our legacy in the generic API sector spans over 80 years. Situated in close proximity to Tel Aviv, Israel, TAPI boasts a workforce of over 5,000 professionals spread across 19 facilities worldwide. Our cutting-edge manufacturing plants are situated in Italy, Hungary, the Czech Republic, Croatia, Israel, India, China, Mexico, and several other locations.

  • Small logo of Lupin

    Lupin

    Manufacturer
    Audited
    Audit report available
    Warning letter

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia
    Flag of United States of AmericaUnited States of America
    Flag of United KingdomUnited Kingdom

    Regulatory compliance

    EDQM
    WHO GMP
    KDMF
    EU WC
    FDA
    JDMF
    GDUFA
    USDMF
    CEP COS
    NDC API

    Audit standards

    GMP (APIs)

    Company description

    Headquartered in Mumbai, India, Lupin is a global pharmaceutical leader with a footprint across the U.S., LATAM, APAC, EMEA and India, with products distributed in over 100 markets. With a diverse portfolio of over 1,200 products, Lupin remains committed to its mission of making quality healthcare accessible to the communities we serve. Our visionary Founder, Dr. Desh Bandhu Gupta, instilled in us the importance of offering quality, affordable and innovative medicines and being a responsible corporate citizen, making a positive difference to patients, communities and the environment.

  • Small logo of Polpharma Group

    Polpharma Group

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of PolandPoland

    Sites

    Flag of AlbaniaAlbania
    Flag of PolandPoland
    Flag of South KoreaSouth Korea
    Flag of IndiaIndia

    Regulatory compliance

    GMP
    JDMF
    KDMF
    NDC API
    USDMF
    CEP COS

    Audit standards

    GMP (Finished Dosage)

    Company description

    Polpharma Group serves as a top-tier pharmaceutical manufacturer in Europe and a reliable partner for pharmaceutical firms globally. With a wide range of products (Rx, CHC, APIs), expert services, and competencies across the value chain, along with extensive knowledge of local CEE/CIS markets, it provides distinct growth opportunities for B2B partners. Collaborating with Polpharma Group offers access to a supportive environment, guidance from skilled professionals, and cutting-edge resources. The company actively seeks partners across various areas of operation, from product development and production to commercial cooperation. Additionally, Polpharma API, a Poland-based CDMO specializing in active pharmaceutical ingredients (APIs), stands as a significant European API supplier, catering to pharmaceutical companies worldwide. The company is in the process of a $45 million manufacturing expansion, incorporating HPAPI and cryogenic technologies, with investments in a pilot plant and R&D capabilities. Operations are set to expand from mid-2023, with full completion expected by 2026.

  • Small logo of Biocon

    Biocon

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia

    Regulatory compliance

    EDQM
    EU WC
    GDUFA
    JDMF
    KDMF
    FDA
    GDP
    NDC API
    USDMF
    CEP COS

    Audit standards

    GMP (APIs)

    Company description

    Founded in 1978, Biocon Limited is the largest biotechnology company in India and a leading company in Asia, focusing on biopharmaceuticals and research services. It is an integrated and innovation-driven enterprise that provides affordable solutions for chronic diseases globally. The company develops, manufactures, and offers a diverse portfolio of Small Molecules APIs & Formulations and Complex Biologics, including Novels and Biosimilars like MAbs, rh-insulin& Insulin Analogs. Among its notable products are the world's first Pichia-based recombinant human Insulin, INSUGEN, Glargine, BASALOG, and India's first biologic BioMAb-EGFR for head and neck cancer. Additionally, it has developed Itolizumab, a 'first in class' anti-CD6 monoclonal antibody, introduced as Alzumab for psoriasis in India in 2013.

  • Small logo of Honour Lab

    Honour Lab

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia

    Regulatory compliance

    EU WC
    KDMF
    JDMF
    FDA
    NDC API
    USDMF
    CEP COS

    Audit standards

    GMP (APIs)

    Company description

    Honour Lab Limited is based in India. The corporation's primary activity involves the production, crafting, or refinement of medications in pharmaceutical formulations for human or animal application.

  • Small logo of Apotex

    Apotex

    Manufacturer

    Headquarters

    Flag of CanadaCanada

    Sites

    Flag of CanadaCanada
    Flag of NetherlandsNetherlands
    Flag of BahamasBahamas
    Flag of IndiaIndia
    Flag of SwitzerlandSwitzerland
    Flag of MexicoMexico
    Flag of BelgiumBelgium

    Regulatory compliance

    EDQM
    WHO GMP
    FDA
    GDUFA
    KDMF
    EU WC
    JDMF
    USDMF
    CEP COS
    NDC API

    Company description

    For more than 40 years, Apotex has been a reputable name in the Canadian pharmaceutical industry, offering patients increased availability to high-quality, cost-effective medications

  • HEC Pharm

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of People's Republic of ChinaPeople's Republic of China

    Sites

    Flag of People's Republic of ChinaPeople's Republic of China

    Regulatory compliance

    EDQM
    KDMF
    JDMF
    USDMF
    CEP COS
    NDC API

    Audit standards

    GMP (APIs)

    Company description

    HEC Pharm Co has obtained approval from the FDA and EDQM as a pharmaceutical manufacturer of both active pharmaceutical ingredients (API) and dosage forms. Presently, HEC is the largest global producer of Macrolides API, including Erythromycin and its derivatives. Sunshine Lake Pharma Co, a subsidiary of HEC Pharm, was established to supply finished pharmaceuticals (dosage forms) to the markets of the United States and European Union (EU).

  • Small logo of Cadila Pharmaceuticals

    Cadila Pharmaceuticals

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia

    Regulatory compliance

    EDQM
    KDMF
    JDMF
    EU WC
    FDA
    GDUFA
    NDC API
    USDMF
    CEP COS

    Audit standards

    GMP (APIs)

    Company description

    Cadila Pharmaceuticals Ltd. is one of the largest privately-held pharmaceutical companies in India. Over the past seven decades, we have been developing and manufacturing affordable medicines for patients around the world. Our innovation-led drug discovery processes ensure the health and well-being of people around the world. Our enhanced investment in innovation and a strong track record in research and development have produced medical miracles that have changed lives and made a profound impact on real life.

  • Optimus Drugs Pvt Ltd.

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia

    Regulatory compliance

    GDUFA
    EU WC
    WHO GMP
    KDMF
    USDMF
    NDC API
    CEP COS

    Audit standards

    GMP (APIs)

    Company description

    Optimus is one of the fastest-growing pharmaceutical companies with 16 years of experience in providing the best quality of API, Intermediates & Finished formulations in Global markets. Our aim from day one has been to provide and ensure better healthcare across the globe through our research, Innovations, affordable products & manufacturing excellence. Sekhmet Pharmaventures acquired major stake in Optimus Drugs Group of Companies in May 2022.

  • Small logo of MSN Life Sciences Pvt. Ltd.

    MSN Life Sciences Pvt. Ltd.

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia

    Regulatory compliance

    EDQM
    EU WC
    GDUFA
    KDMF
    JDMF
    FDA
    USDMF
    NDC API
    CEP COS

    Audit standards

    GMP (APIs)
    GMP (Finished Dosage)

    Company description

    MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible.

  • Small logo of Morepen Laboratories

    Morepen Laboratories

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia

    Regulatory compliance

    EDQM
    WHO GMP
    GDUFA
    EU WC
    KDMF
    JDMF
    FDA
    USDMF
    CEP COS
    NDC API

    Audit standards

    GMP (APIs)

    Company description

    Embarking on a transformative journey over four decades, Morepen has consistently strived to embody an organization marked by discernible, impactful differences. Every action we undertake is imbued with a profound commitment to enrich the lives we touch. Nestled amidst the serene surroundings of Baddi, our cutting-edge manufacturing facility boasts a scientifically integrated complex housing 10 plants, each tailored to produce specific product lines. Driven by a relentless pursuit of innovation, Morepen's extensive research and development infrastructure, alongside our dedicated workforce, ensures the maintenance of stringent quality standards. With a robust global footprint, we export to over 80 countries, holding certifications from esteemed regulatory authorities such as USFDA, WHO GMP, and EU GMP.

  • Small logo of Macleods Pharmaceuticals

    Macleods Pharmaceuticals

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia

    Regulatory compliance

    EDQM
    WHO GMP
    EU WC
    FDA
    KDMF
    GDUFA
    USDMF
    CEP COS
    NDC API

    Audit standards

    GMP (Finished Dosage)
    GMP (APIs)
  • Sintenovo

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of MexicoMexico

    Sites

    Flag of MexicoMexico

    Regulatory compliance

    KDMF
    FDA
    USDMF
    CEP COS
    NDC API

    Audit standards

    GMP (APIs)

    Company description

    Sintenovo, the Mexican branch of Esteve Quimica from Spain, is dedicated to the development, manufacturing, and marketing of advanced intermediates and API’s for various markets including Mexico, the US, and Europe. Sintenovo’s multipurpose plant in Jiutepec adheres to cGMP standards and has a total capacity of 140 m3. It has successfully passed inspections and received approval from the FDA, PMDA, as well as the Mexican and EU authorities.

  • Small logo of Amoli Organics

    Amoli Organics

    Manufacturer
    Audited
    Audit report available
    Non-Compliance Report

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia

    Regulatory compliance

    EDQM
    WHO GMP
    KDMF
    EU WC
    GDUFA
    FDA
    JDMF
    CEP COS
    USDMF
    NDC API

    Audit standards

    GMP (APIs)

    Company description

    Amoli has been working collaboratively with some of the leading global healthcare players since 3 decades. Our strength comes from our expertise in process chemistry further bolstered by our EDQM and USFDA approved facilities allowing us to cater to the needs of the pharmaceutical industry globally. We offer APIs from a wide range of therapeutic classes like NSAIDS, Antifungals, Antidepressants, Hypolipidemics etc. With the support our state-of-the-art R&D centre, we are constantly expanding our product range and foraying into newer therapeutic categories.

  • Small logo of Moehs Iberica

    Moehs Iberica

    Manufacturer
    Audited

    Headquarters

    Flag of SpainSpain

    Sites

    Flag of SpainSpain

    Regulatory compliance

    EDQM
    KDMF
    JDMF
    USDMF
    CEP COS
    NDC API

    Company description

    Moehs Ibérica is the headquarters of the MOEHS Group. Moehs Ibérica currently has 138 employees in the following departments: Accounting/Treasury, Purchasing/Logistics, Sales/Marketing, Human Resources, IT, Quality Assurance/Regulatory Affairs, Research and Intellectual Property. It provides services to the entire group and each of its subsidiaries. In addition, it has its own R&D building with all its services and a plant dedicated to the production of small quantities of ingredients for the pharmaceutical industry, as well as a plant for the manufacture of High Potency Active Ingredients.

  • Wockhardt

    Manufacturer
    Audited
    Non-Compliance Report

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia
    Flag of IrelandIreland
    Flag of United KingdomUnited Kingdom
    Flag of United States of AmericaUnited States of America

    Regulatory compliance

    EDQM
    WHO GMP
    KDMF
    JDMF
    EU WC
    FDA
    GDUFA
    CEP COS
    USDMF

    Company description

    Wockhardt UK (WUK) operates as a diverse pharmaceutical company, serving as a significant provider of healthcare products to the NHS through hospitals, multiple retail pharmacy chains, and wholesalers. It is currently experiencing an exciting period with thriving export and contract manufacturing divisions. Leveraging the global strength, research base, and impressive product pipeline of its parent company, Wockhardt UK is well-positioned for future growth.

  • Small logo of Zhejiang Jiuzhou Pharmaceutical

    Zhejiang Jiuzhou Pharmaceutical

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of People's Republic of ChinaPeople's Republic of China

    Sites

    Flag of People's Republic of ChinaPeople's Republic of China

    Regulatory compliance

    EDQM
    FDA
    JDMF
    KDMF
    GDUFA
    USDMF
    CEP COS
    NDC API

    Audit standards

    GMP (APIs)

    Company description

    Zhejiang Jiuzhou Pharmaceutical Co., Ltd. (Abbreviated Name: Jiuzhou Pharma, Stock Code: 603456.SH), founded in 1998 and headquartered in Taizhou, Zhejiang, is a leading contract development and manufacturing organization (CDMO) that successfully evolved from a generic API manufacturer. We provide pharmaceutical companies worldwide with one-stop innovative drug development and manufacturing solutions and services throughout the development lifecycle of an innovative drug—from preclinical chemical manufacturing and control (CMC) through phase I/II/III clinical trials and new drug applications (NDA) to commercialization. As a leader in green pharmaceutical manufacturing, we have developed frontier environmentally-friendly pharmaceutical technologies with independent intellectual property rights. We are committed to providing our customers with industry-leading technical solutions that enhance R&D efficiency and success while reducing costs. Serve life, guard health. We are committed to becoming a distinguished global life science company that provides innovative drug solutions to help our partners accelerate the time to market of innovative drugs and benefit patients worldwide.

  • Small logo of Uquifa

    Uquifa

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of SpainSpain

    Sites

    Flag of SpainSpain
    Flag of MexicoMexico

    Regulatory compliance

    EDQM
    JDMF
    KDMF
    USDMF
    CEP COS
    NDC API

    Audit standards

    GMP (APIs)

    Company description

    Bringing 86 years of expertise, UQUIFA'S operational approach is built on a fusion of a high-quality production platform and a proven history of service and dependability. UQUIFA specializes in the production of Active Pharmaceutical Ingredients (APIs), Intermediates, and RSM's for the pharmaceutical and animal health sectors on a global scale. The organization runs 2 production facilities (located in Spain and Mexico) with stringent compliance to all regulatory standards. These facilities operate under cGMP conditions and have undergone evaluation and endorsement from prominent global pharmaceutical companies.

  • Small logo of Lee Pharma

    Lee Pharma

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia

    Regulatory compliance

    EDQM
    KDMF
    EU WC
    WHO GMP
    JDMF
    FDA
    NDC API
    USDMF
    CEP COS

    Audit standards

    GMP (APIs)

    Company description

    Lee Pharma Limited was established in 1997 in India it is a research-driven company with a critical focus on the development, synthesis, and commercialization of new products and cost-effective processes. ​ We manufacture several intermediate chemicals, Active Pharmaceutical Ingredients & Semi-finished Dosage Forms (Pellets & Granules), and Finished Formulations. Our expertise in the field won us, numerous clients, in India as well as across the globe. Lee Pharma Manufacturing facilities are approved by several international regulatory bodies such as USFDA, EUGMP, WHO GMP etc.

  • Small logo of Viatris

    Viatris

    Manufacturer

    Headquarters

    Flag of United States of AmericaUnited States of America

    Sites

    Flag of United States of AmericaUnited States of America
    Flag of CanadaCanada
    Flag of IrelandIreland
    Flag of IndiaIndia
    Flag of PolandPoland
    Flag of Puerto RicoPuerto Rico
    Flag of AustraliaAustralia

    Regulatory compliance

    WHO GMP
    FDA
    GDUFA
    EDQM
    GDP

    Company description

    VIATRIS™ represents a fresh approach to healthcare, dedicated to ensuring medicine accessibility, promoting sustainable practices, pioneering creative remedies, and enhancing patient results. Founded in 2020 through the merger of Mylan and Upjohn, Viatris unites top-notch scientific, production and distribution skills with established regulatory, medical and commercial proficiencies.

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