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    Pharmaceutical manufacturers of Sumatriptan

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

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    26results for pharmaceutical manufacturers of Sumatriptan

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    • Small logo of Chromo Laboratories

      Chromo Laboratories

      Manufacturer
      Audited
      Audit report available

      Sites

      Flag of IndiaIndia
      Flag of PolandPoland

      Regulatory compliance

      FDA
      GDUFA
      EU WC
      CEP COS
      NDC API
      USDMF

      Audit standards

      GMP (APIs)

      Company description

      Chromo Labs operates as a fully integrated pharmaceutical company, engaging in international, active pharmaceutical ingredient (API), and oral solid dosage (OSD) manufacturing. With approvals from USFDA, EDQM, WHO GENEVA, COFEPRIS, ANVISA, and EUWC, Chromo API holds 19 CEP approvals and has 7 CEPs under review. Additionally, Chromo API has filed 35 USDMFs, 6 of which are currently commercialized. The company possesses a comprehensive backup API portfolio, supported by Chromo Medcare and Gensynth Pharmachem.

    • 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 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.

    • Small logo of Natco Pharma

      Natco Pharma

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of IndiaIndia

      Sites

      Flag of IndiaIndia
      Flag of ThailandThailand

      Regulatory compliance

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

      Audit standards

      GMP (APIs)
      GMP (Finished Dosage)

      Company description

      Natco Pharma Limited was incorporated in Hyderabad in the year 1981 with an initial investment of INR 3.3 million. With a modest beginning of operations as a single unit with 20 employees, Natco today has eight manufacturing facilities spread across India with dedicated modern research laboratories, capabilities in New Drug Development, etc. Natco family currently consists of around 4500 employees, we are consistently ranked among fastest growing pharmaceutical companies in India. Natco is well recognized for its innovation in Pharmaceutical R&D.

    • Small logo of Sun Pharmaceutical Industries

      Sun Pharmaceutical Industries

      Manufacturer
      Audited
      Audit report available
      Warning letter

      Headquarters

      Flag of IndiaIndia

      Sites

      Flag of IndiaIndia
      Flag of AustraliaAustralia
      Flag of NetherlandsNetherlands
      Flag of United States of AmericaUnited States of America
      Flag of United KingdomUnited Kingdom
      Flag of HungaryHungary
      Flag of IsraelIsrael
      Flag of IrelandIreland
      Flag of CanadaCanada

      Regulatory compliance

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

      Audit standards

      GMP (APIs)
      GMP (Finished Dosage)

      Company description

      Sun Pharma is a global, comprehensive, specialized pharmaceutical company with production facilities for API and FDF in India, the United States, Latin America, and Europe. It produces and sells a wide range of pharmaceutical formulations as branded generics and generic drugs in India, the US, and various other global markets. It is supported by 2 advanced R&D Centers with a team of over 600 scientists for projects in Chemical Synthesis, Clinical Research, and formulation development. Sun is a frontrunner in specific therapy areas and possesses robust expertise in product development, process chemistry, and manufacturing.

    • 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.

    • Nosch Labs

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of IndiaIndia

      Sites

      Flag of IndiaIndia

      Regulatory compliance

      EDQM
      EU WC
      KDMF
      JDMF
      CEP COS
      USDMF

      Audit standards

      GMP (APIs)
      GMP (Finished Dosage)

      Company description

      Dream that drives us at Nosch. The laudable goal that we aim for. The vision that suffuses us with the passion to innovate and excel. Over the past twenty one years, we have been ceaselessly engaged in a quest to sustain and improve the quality of life through creating safe pharmaceutical solutions. Our competencies have grown to embrace the entire pharmaceutical value chain-APIs and semi-finished Formulations. Today, with an impeccable reputation for uncompromising quality and timely delivery, Nosch has emerged as the partner of choice across the world.

    • Small logo of SMS Pharmaceuticals

      SMS Pharmaceuticals

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of IndiaIndia

      Sites

      Flag of IndiaIndia

      Regulatory compliance

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

      Audit standards

      GMP (APIs)

      Company description

      SMS Lifesciences India Limited, headquartered in Hyderabad, India, is a research-driven company with over three decades of experience. It is a public listed leading API manufacturer, supplying to major generic and innovator firms. With a focus on APIs, the company operates four state-of-the-art facilities and provides quality alternative manufacturing solutions to multinational companies for their contract research and manufacturing needs. The company has multiple manufacturing facilities supporting a wide range and capacity of APIs and Intermediates.

    • Small logo of Orchid Pharma

      Orchid Pharma

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of IndiaIndia

      Sites

      Flag of IndiaIndia

      Regulatory compliance

      EDQM
      WHO GMP
      GDUFA
      FDA

      Audit standards

      GMP (APIs)

      Company description

      Founded in 1992 as an export-centric unit (EOU), Orchid Pharma Ltd. (Orchid) is an integrated company covering the entire pharmaceutical value chain from exploration to distribution with established expertise in research, production, and promotion. Presently, we are listed among the top 50 pharmaceutical firms in India and have a diverse presence in various therapeutic areas including anti-infectives, anti-inflammatory, central nervous system (CNS), cardiovascular segment (CVS), nutraceuticals, and other oral and sterile products.

    • Small logo of Hovione

      Hovione

      Manufacturer

      Headquarters

      Flag of PortugalPortugal

      Sites

      Flag of People's Republic of ChinaPeople's Republic of China
      Flag of PortugalPortugal
      Flag of MacaoMacao
      Flag of United States of AmericaUnited States of America
      Flag of IrelandIreland

      Regulatory compliance

      EDQM
      GDUFA
      FDA
      JDMF
      KDMF
      USDMF
      NDC API
      CEP COS

      Company description

      Hovione brings over six decades of experience as a CDMO and serves as a specialized integrated provider delivering solutions for drug substance, drug product intermediate, and drug product. With four FDA examined facilities in the United States, China, Ireland, and Portugal, as well as research laboratories in Portugal and the United States, the company supplies pharmaceutical customers with services for the development and compliant production of innovative drugs, including highly potent compounds. Hovione delivers a comprehensive range of development services and manufacturing capabilities in particle engineering such as Spray Drying.

    • Small logo of Shandong Xinhua Pharmaceutical

      Shandong Xinhua 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
      Flag of United States of AmericaUnited States of America

      Regulatory compliance

      EDQM
      FDA
      KDMF
      JDMF
      GDUFA
      GDP
      CEP COS
      NDC API
      USDMF

      Audit standards

      GMP (APIs)

      Company description

      Shandong Xinhua was founded in 1943. After evolving for more than 75 years, it has established 5 manufacturing facilities, spanning an area of over 3 million square meters. The company has set up two international branches and employs over 5000 staff. Its business encompasses API, finished dosage formulation, pharmaceutical intermediates, and pharmaceutical commerce.

    • Srini Pharmaceuticals

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of IndiaIndia

      Sites

      Flag of IndiaIndia

      Regulatory compliance

      EU WC
      KDMF
      JDMF
      FDA
      GDUFA
      USDMF
      NDC API
      CEP COS

      Audit standards

      GMP (APIs)

      Company description

      Srini Pharmaceuticals Pvt. Ltd., was established in 1995. USFDA, TGA and KFDA approved fully integrated global pharmaceutical company, located just about 60 KM's away from the Pharma Capital of India, Hyderabad. Our manufacturing facility has five fully equipped production blocks with most efficient functional utilities with multiple clean rooms having the ability to produce 10 API's at a time, supported by central quality control laborites with all sophisticated instruments by maintaining complete QMS. The state-of-the-Art Research and development laboratory recognized and approved by Department of Science and Technology, Government of India.

    • Small logo of Smilax Laboratories

      Smilax Laboratories

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of IndiaIndia

      Sites

      Flag of IndiaIndia

      Regulatory compliance

      JDMF
      WHO GMP
      EDQM
      EU WC
      NDC API
      CEP COS
      USDMF

      Audit standards

      GMP (APIs)

      Company description

      Smilax Laboratories Limited is a leading vertically integrated pharmaceutical organization, manufacturing Active Pharmaceutical Ingredients, API Intermediates and NDDS/Pellets for the generics market across the world. The position today built by Smilax is due to its cutting edge research , world class manufacturing and a truly global supply chain management.

    • Sm Biomed

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of MalaysiaMalaysia

      Sites

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

      Regulatory compliance

      KDMF
      FDA
      CEP COS
      NDC API
      USDMF

      Audit standards

      GMP (APIs)

      Company description

      Established in the year 1991, SM Biomed Sdn. Bhd. is a leading manufacturer of Active Pharmaceutical Ingredients (APIs) and Intermediates based out in Malaysia With our state-of-the-art manufacturing facility certified by USFDA, EDQM, EUGMP and NPRA (Malaysia), we are dedicated to improve the quality of life through developing and delivering innovative solutions and products at an affordable cost. With a legacy spanning more than three decades and pioneers for Macrolide based antibiotics, we work with customers globally with speed, efficiency and cost effective manufacturing capabilities. SM Biomed has grown as a market leader in Macrolides antibiotics and evolved into a knowledge driven company providing reliable pharmaceutical services including developing and manufacturing APIs and Intermediates. From pipeline to production, we make innovative, quality driven and customised products more accessible. We are a quality driven and R&D focused API manufacturing company with a diverse product portfolio catering various therapeutic segments.

    • Small logo of Sintetica

      Sintetica

      Manufacturer
      Audited

      Headquarters

      Flag of SwitzerlandSwitzerland

      Sites

      Flag of SpainSpain
      Flag of SwitzerlandSwitzerland

      Regulatory compliance

      JDMF
      KDMF
      GDUFA
      EDQM
      FDA
      GDP
      USDMF
      NDC API
      CEP COS
    • Small logo of Synergene Active Ingredients

      Synergene Active Ingredients

      Manufacturer

      Headquarters

      Flag of IndiaIndia

      Sites

      Flag of IndiaIndia

      Regulatory compliance

      EU WC
      JDMF
      FDA
      CEP COS
      USDMF
    • Vamsi Labs

      Manufacturer

      Headquarters

      Flag of IndiaIndia

      Sites

      Flag of IndiaIndia

      Regulatory compliance

      EU WC
      FDA
      WHO GMP
      NDC API
      CEP COS
      USDMF

      Company description

      Vamsi Labs, founded in 1991, is a prominent Indian producer of active pharmaceutical ingredients (API). It specializes in anti-asthmatic, anti-migraine, and anti-psychotic APIs, serving both domestic and international markets with 50% sales contribution from the latter. Sales of anti-asthma products make up 60% of the total sales. Vamsi upholds stringent corporate governance, transparency, professionalism, and environmental conservation standards. The company is approved by USFDA and holds certifications for ISO 9001:2015, ISO 14001:2015, and ISO 45001:2018. It also features a DSIR-certified R&D Lab, allowing Vamsi to continue innovating to meet the evolving requirements of the pharmaceutical industry. Vamsi is positioned for global expansion while maintaining its dedication to excellence and sustainability.

    • Small logo of Maithili Life Sciences

      Maithili Life Sciences

      Manufacturer

      Headquarters

      Flag of IndiaIndia

      Sites

      Flag of IndiaIndia

      Regulatory compliance

      KDMF
      CEP COS
      NDC API
      USDMF

      Company description

      Maithili Life Sciences offers services including DMF, CEP, Written Confirmations, FDF, Prices, Patents, Patents & Exclusivities, Dossier, Manufacturer, Licensing, Distributer, Suppliers, and News related to GMP.

    • Small logo of Hunan Jiudian Hongyang Pharmaceutical

      Hunan Jiudian Hongyang 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
      Flag of South KoreaSouth Korea

      Regulatory compliance

      GMP
      KDMF
      NDC API
      USDMF

      Audit standards

      GMP (APIs)

      Company description

      Established in 2001, Hunan Jiudian Pharmaceutical Co., Ltd. is a contemporary GMP pharmaceutical and publicly traded company specializing in finalized products, active pharmaceutical ingredients (APIs), excipients, traditional Chinese medicine, and nutritional supplements. Boasting 2 facilities, 400 researchers, and a total of 1,900 employees, the company's primary products are all independently researched by its own team, encompassing analgesic drugs, cardio-cerebrovascular treatments, anti-infection solutions, digestive and urinary system aids, as well as respiratory and anti-allergy products. Additionally, Hunan Jiudian Hongyang Pharmaceutical Co., Ltd. functions as a wholly-owned subsidiary of Jiudian, focusing on the production of APIs and excipients.

    • Therapiva

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of IndiaIndia

      Sites

      Flag of IndiaIndia

      Regulatory compliance

      KDMF
      EU WC
      JDMF

      Audit standards

      GMP (APIs)

      Company description

      Therapiva is a prominent manufacturer of generic pharmaceuticals with a strong and innovative R&D center and a state-of-the-art API manufacturing plant. It offers a diverse product range spanning various medical areas and is capable of managing novel, intricate, and high-risk reactions. Therapiva provides new chemical entities (NCEs), cGMP intermediates, and key starting materials (KSMs) to global innovators. The company is furnished with adaptable, multi-faceted, and advanced infrastructure, customized to accommodate the production of complex molecular chemistry emerging from Innovator's development pipelines.

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