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    Pharmaceutical manufacturers of Sofosbuvir

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

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    18results for pharmaceutical manufacturers of Sofosbuvir

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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 Farmak International

      Farmak International

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of SwitzerlandSwitzerland

      Sites

      Flag of UkraineUkraine

      Regulatory compliance

      EDQM
      FDA

      Audit standards

      GMP (Finished Dosage)
    • Small logo of Virupaksha Organics

      Virupaksha Organics

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of IndiaIndia

      Sites

      Flag of IndiaIndia

      Regulatory compliance

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

      Audit standards

      GMP (APIs)

      Company description

      VIRUPAKSHA ORGANICS LIMITED operates as a fully integrated manufacturer of Active Pharmaceutical Ingredients (API’s) and intermediates in Hyderabad, Telangana, India. The company is overseen by professionals from the pharmaceutical industry with over 25 years of expertise. The successful combination of technical knowledge, organizational capabilities, experience, and infrastructure has contributed to the company's achievements and expansion. Established in 2003, the company achieved an impressive turnover of USD 30 million in its 10th year of operation.

    • Small logo of Laurus Labs

      Laurus Labs

      Manufacturer
      Audited

      Sites

      Flag of IndiaIndia
      Flag of United KingdomUnited Kingdom

      Regulatory compliance

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

      Company description

      In just over a decade, Laurus has positioned itself as one of the largest and most innovative API producers globally. Expanding upon its established expertise in chemistry, Laurus has recently adopted full vertical integration, including a strong finished dosage capacity, dedicated capacity for backward integration, and also Synthesis R&D operations in India and the USA.

    • Small logo of Cambrex

      Cambrex

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of United States of AmericaUnited States of America

      Sites

      Flag of SwedenSweden
      Flag of United States of AmericaUnited States of America
      Flag of ItalyItaly

      Regulatory compliance

      EDQM
      KDMF
      JDMF
      FDA
      GDUFA
      GDP
      USDMF
      NDC API
      CEP COS

      Audit standards

      GMP (APIs)

      Company description

      Cambrex stands as a prominent global contract development and manufacturing organization (CDMO) delivering comprehensive analytical and IND enabling services, along with drug substance development and manufacturing throughout the entire drug lifecycle. Boasting 40 years of expertise and a workforce of 2,000 professionals catering to international clients from North America and Europe, Cambrex is a reliable ally in both the branded and generic markets for API development and manufacturing. The company provides a variety of specialized drug substance technologies and capabilities.

    • 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 Changzhou Pharmaceutical Factory

      Changzhou Pharmaceutical Factory

      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
      FDA
      GDUFA
      USDMF
      CEP COS
      NDC API

      Audit standards

      GMP (APIs)

      Company description

      Changzhou Pharmaceutical Factory (CPF) is a subsidiary company of Shanghai Pharma Holdings Co., Ltd., It is headquartered in Changzhou, Jiangsu province, China, Changzhou pharmaceutical Factory has a rich history & Lineage in the pharmaceutical sector. The company was founded in 1949 by (Tan Ruiting) with a registered capital 108 million yuan and the company was restructured as a Changzhou pharmaceutical Factory under the aegis of Shanghai Pharma Group. The Chinese business of Changzhou pharmaceutical factory was full fledged sales & marketing organization,Changzhou Pharma is a one of the prominent players in the Chinese pharmaceutical formulations market with a strong foothold across multiple therapies. The company have more than 1500 employees across the country and has earned a reputation amongest the Chinese pharmaceutical companies for providing innovative, comprehensive and complete healthcare solutions. At Changzhou pharmaceutical Factory, we have one of the strongest global commercial infrastructures in the industry, with a balanced reach across US, Europe, the Asia Pacific region and emerging markets. Our high quality manufacturing dedicated facilities for Oncology, Non Oncology, Complex Generics, OTC-Products and sterile injectables, scientific excellence and vast supply chain network to improve access to medicine for patients worldwide. The company mainly involves leading pharmaceutical manufacturer a wide range of key Intermediates, Active pharmaceutical ingredients, Finished Formulations meet with global standards, Changzhou Pharmaceutical Factory it covers an area of 300,000㎡ including R&D, dedicated manufacturing, international marketing office. And we maintain an industry -leading pipeline, composed of numerous complex generics and state owned brands. The company annually brings 800 tons of API's and 3000 millions of Finished dosage forms across the Globe.

    • Dong-A ST

      Manufacturer

      Headquarters

      Flag of South KoreaSouth Korea

      Sites

      Flag of South KoreaSouth Korea
      Flag of People's Republic of ChinaPeople's Republic of China

      Regulatory compliance

      JDMF
      KDMF
      EDQM
      USDMF
      CEP COS
      NDC API

      Company description

      Dong-A has held the position of the largest pharmaceutical company in Korea since 1967. Our predominant market presence is attributed to internally developed products such as Suganon tab, Evogliptin, which is a DPP-4 inhibitor for type 2 diabetes mellitus, Zydena tab, which is Udenafil, the fourth PDE5 inhibitor globally for erectile dysfunction, Stillen tab, a herbal treatment for gastritis with Eupatilin, and Motilitone tab, which contains Corydaline for functional dyspepsia. Additionally, we provide branded generic drugs (anti-cancer, anti-TB, etc.), bio-pharmaceutical, IMD, APIs, and OTC products.

    • Small logo of Haoyuan Chemexpress

      Haoyuan Chemexpress

      Manufacturer

      Regulatory compliance

      USDMF
    • Small logo of St Pharm

      St Pharm

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of South KoreaSouth Korea

      Sites

      Flag of South KoreaSouth Korea

      Regulatory compliance

      FDA
      GMP
      ISO
      EDQM
      USDMF
      KDMF
      NDC API
      CEP COS
      JDMF

      Audit standards

      GMP (APIs)

      Company description

      ST Pharm has provided exceptional custom production services for oligonucleotides and small molecule APIs CDMO to fulfill clients’ elevated requirements in pharmaceutical development while adhering to cGMP regulations. The enhancement of oligonucleotide manufacturing capabilities has emerged as a new driving force for the future of the pharmaceutical industry

    • American Pacific

      Manufacturer

      Headquarters

      Flag of United States of AmericaUnited States of America

      Sites

      Flag of United States of AmericaUnited States of America
      Flag of IrelandIreland

      Regulatory compliance

      EDQM
      KDMF
      FDA
      GDUFA
      NDC API
      CEP COS
      USDMF
    • Small logo of Jiangsu Yutian Pharmaceutical

      Jiangsu Yutian 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

      CEP COS

      Audit standards

      GMP (APIs)

      Company description

      As a new characteristic API and CDMO pharmaceutical enterprises specializing in the development, production and sales of modern medicines, Jiangsu Yutian Pharmaceutical Co., Ltd. is committed to providing high-quality APIs and Intermediates to major pharmaceutical companies in China, and our products are also well sold in Europe, Japan, South Korea, India and other dozens of countries. Now, we are one of the key national high-tech enterprises of China, a small science and technology giant enterprise of the city, and a backbone enterprise of the new pharmaceutical industry base of China Pharmaceutical Port.

    • Jiangsu Coben 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

      Audit standards

      GMP (APIs)

      Company description

      Established in 2005, Coben Group was created and constructed in accordance with GMP standard covering a total area of 100,000 square meters. It is a part of ZJMI Group-Global Fortune 500, achieving the 270th position in 2018. Coben specializes in the research and production of APIs and intermediates for a variety of medications. Its primary products consist of Sofosbuvir, Tenofovir, Ticagrelor, Sacubitril, Voriconazole, Isavuconazole, and their respective intermediates.

    • Fuxin Long Rui Pharmaceutical

      Manufacturer

      Headquarters

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

      Regulatory compliance

      USDMF
    • Small logo of Cad Middle East Pharmaceutical Industries

      Cad Middle East Pharmaceutical Industries

      Manufacturer

      Headquarters

      Flag of Saudi ArabiaSaudi Arabia

      Regulatory compliance

      CEP COS
    • Topharman Shandong

      Manufacturer

      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
    • Beijing Huikang Boyuan Chemical Tech

      Manufacturer

      Headquarters

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

      Regulatory compliance

      USDMF
    • Ampac Fine Chemicals

      Manufacturer

      Sites

      Flag of United States of AmericaUnited States of America

      Regulatory compliance

      EDQM
      KDMF
      CEP COS
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