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Pharmaceutical manufacturers of Losartan

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69results for pharmaceutical manufacturers of Losartan

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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 Flamma

    Flamma

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of ItalyItaly

    Sites

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

    Regulatory compliance

    EDQM
    KDMF
    JDMF
    GDUFA
    FDA
    USDMF
    NDC API
    CEP COS

    Audit standards

    GMP (APIs)

    Company description

    FLAMMA is a CDMO based near Milan, Italy. As a fully integrated CDMO, we can utilize our 100% self-owned, self-managed facilities, in Italy and China to ensure a stable, dependable supply chain. Our specialization lies in the cGMP manufacturing of APIs, NCEs, RSMs, and advanced intermediates, including high value chiral materials such as amino acid related materials. We also offer manufacturing of specialty compounds and advanced intermediates to meet the diverse needs of our clients.

  • 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 Unichem Laboratories

    Unichem Laboratories

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia
    Flag of SpainSpain

    Regulatory compliance

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

    Audit standards

    GMP (APIs)
    GMP (Finished Dosage)

    Company description

    Unichem Laboratories was founded in 1944 by Late Mr. Amrut Mody, a pioneer in the Indian pharmaceuticals business. With a rich tradition of unwavering quality and reliability, Unichem brings together a unique blend of modern, value-added research and deep knowledge of the Indian pharmaceuticals industry.ç

  • Small logo of Zhejiang Hisun Pharmaceutical Co., Ltd

    Zhejiang Hisun Pharmaceutical Co., Ltd

    Manufacturer
    Audited
    Audit report available
    Non-Compliance Report

    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 JapanJapan

    Regulatory compliance

    EDQM
    GDUFA
    CE
    KDMF
    FDA
    JDMF
    CEP COS
    NDC API
    USDMF

    Audit standards

    GMP (APIs)

    Company description

    Founded in 1956, Zhejiang Hisun Pharmaceutical Co., Ltd. is a comprehensive pharmaceutical enterprise featuring whole chain, multi-regional integration of research, production and marketing as well as development of drug substances and preparations. In 2000, an A-share was issued in order to enter the stock market as a state-owned listed company. As of 2021, Hisun Pharmaceutical is now one of the largest producers of antibiotics and anti-tumor drugs in China and has been listed in the Top 500 Chinese manufacturing enterprises and the Top 100 Chinese pharmaceutical enterprises multiple times. In 2020 Hisun Pharmaceuticals received special recognition from the Joint Prevention and Control Team from the State Council of the People’s Republic of China for their extraordinary efforts in the fight against the epidemic, and Hisun Pharmaceutical was awarded with the “Anti COVID-19 Advanced Collective in Ministry of Industry and Information Technology".

  • Small logo of LEK Pharmaceuticals

    LEK Pharmaceuticals

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of SloveniaSlovenia

    Sites

    Flag of SloveniaSlovenia
    Flag of United States of AmericaUnited States of America
    Flag of SpainSpain
    Flag of CanadaCanada
    Flag of AustriaAustria
    Flag of GermanyGermany
    Flag of FranceFrance
    Flag of NetherlandsNetherlands
    Flag of BelgiumBelgium
    Flag of DenmarkDenmark
    Flag of RomaniaRomania
    Flag of ItalyItaly

    Regulatory compliance

    EDQM
    KDMF
    GDUFA
    FDA
    JDMF
    CEP COS
    USDMF
    NDC API

    Audit standards

    GMP (APIs)
    GMP (Finished Dosage)
  • Small logo of Aurobindo Pharma

    Aurobindo Pharma

    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 NetherlandsNetherlands

    Regulatory compliance

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

    Audit standards

    GMP (APIs)
    GMP (Finished Dosage)

    Company description

    Founded in 1986 by Mr. P. V. Ramprasad Reddy, Mr. K. Nityananda Reddy and a small group of highly committed professionals, Aurobindo Pharma was born of a vision. The company commenced operations in 1988-89 with a single unit manufacturing Semi-Synthetic Penicillin (SSP) at Pondicherry. Aurobindo Pharma became a public company in 1992 and listed its shares on the Indian stock exchanges in 1995. In addition to being the market leader in Semi-Synthetic Penicillins, it has a presence in key therapeutic segments such as neurosciences, cardiovascular, anti-retrovirals, anti-diabetics, gastroenterology and anti-biotics, among others.

  • Assia Chemical Industries

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IsraelIsrael

    Sites

    Flag of IsraelIsrael

    Regulatory compliance

    KDMF
    GDUFA
    JDMF
    FDA
    NDC API
    USDMF

    Audit standards

    GMP (APIs)

    Company description

    Teva's roots are deeply rooted in the land of Israel since 1901 in Jerusalem. That's when the first chapter was written in the long and unique history of the company, which slowly transformed from a small drug trading house to the largest generic company in the world, improving the health of millions of patients in Israel and around the world every day.

  • Small logo of Alembic Pharmaceuticals

    Alembic Pharmaceuticals

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia

    Regulatory compliance

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

    Audit standards

    GMP (APIs)

    Company description

    Alembic Pharmaceuticals Limited is involved in manufacturing and marketing India Formulations, International Generics, and Active Pharmaceutical Ingredients with vertical integration capabilities. Headquartered in Vadodara, Gujarat, we derive a third of our revenue of over $600 million from the India market.

  • Small logo of Shilpa Medicare

    Shilpa Medicare

    Manufacturer
    Audited
    Audit report available
    Warning letter

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia
    Flag of PolandPoland

    Regulatory compliance

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

    Audit standards

    GMP (APIs)

    Company description

    We specialize in premium Active Pharmaceutical Ingredients (APIs), Formulations, Innovative Drug Delivery Systems, and Specialty Chemicals using advanced technology with precision to adhere to global standards/specifications. Presently, we are recognized as one of the foremost global providers of Oncology/non-Oncology APIs, intermediates, and Formulations. Shilpa Medicare’s establishments have garnered significant regulatory endorsements from USFDA, EUGMP, TGA, PMDA, Cofepris, Anvisa, and KFDA, encompassing diverse regulatory approved manufacturing standards.

  • Small logo of Zydus Lifesciences

    Zydus Lifesciences

    Manufacturer
    Audited
    Audit report available
    Warning letter

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia
    Flag of FranceFrance
    Flag of United States of AmericaUnited States of America

    Regulatory compliance

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

    Audit standards

    GMP (APIs)

    Company description

    The Zydus group is based in Ahmedabad, India, and is placed 4th in the Indian pharmaceutical sector. Zydus' global operations have a substantial presence in the regulated markets of the US, Europe (specifically France and Spain), and in the prominent markets of Latin America and South Africa. It also has a significant presence in 25 other developing markets around the world.

  • Enaltec Labs

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia

    Regulatory compliance

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

    Audit standards

    GMP (Subcontracted Laboratory)

    Company description

    Enaltec was established in 2006 by a group of young and experienced professionals with the specific objective to develop and produce complex, small volume, technology-driven products at competitive prices, thus providing the critical India advantage to generic formulators across the world.

  • 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.

  • Small logo of Dr. Reddy's Laboratories

    Dr. Reddy's Laboratories

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IndiaIndia

    Sites

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

    Regulatory compliance

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

    Audit standards

    GMP (Finished Dosage)
    GMP (APIs)
    GMP (Excipients)

    Company description

    Dr. Reddy’s Laboratories Ltd. functions as an integrated pharmaceutical firm, dedicated to supplying cost-effective and innovative medications to promote healthier lifestyles. With a focus on Pharmaceutical Services & Active Ingredients, Global Generics, and Proprietary Products, Dr. Reddy’s delivers a range of products and services such as APIs, customized pharmaceutical services, generics, biosimilars, and distinct formulations. The primary therapeutic areas of concentration encompass gastro-intestinal, cardiovascular, diabetology, oncology, pain management, and dermatology. Dr. Reddy’s has a presence in various global markets, with significant engagements in the USA, Europe, India, Russia, and other CIS nations.

  • Small logo of Hetero Drugs

    Hetero Drugs

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia
    Flag of MaltaMalta

    Regulatory compliance

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

    Audit standards

    GMP (Finished Dosage)
    GMP (APIs)

    Company description

    We are one of world’s leading producers of key Active Pharmaceutical Ingredients (APIs) and generic formulations with presence in 140+ countries and backed by 30 years of experience in the pharma sector. We endeavour to serve patients by moulding science and technology into therapies to improve health outcomes and people’s lives.

  • Small logo of Ipca Laboratories

    Ipca Laboratories

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia
    Flag of PolandPoland

    Regulatory compliance

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

    Audit standards

    GMP (APIs)

    Company description

    For more than 60 years, Ipca has been a crucial healthcare partner in over 120 countries across the 6 continents. We are a fully-integrated pharmaceutical company that manufactures over 350 formulations and 80 APIs for various therapeutic segments. Today, we are one of the world’s largest manufacturers and suppliers of over a dozen APIs. These are produced from scratch at fully-automated manufacturing facilities, approved by the world’s most discerning drug regulatory authorities like UK-MHRA, EDQM-Europe, and WHO-Geneva, among others.

  • Small logo of Fareva

    Fareva

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of FranceFrance

    Sites

    Flag of FranceFrance
    Flag of GermanyGermany
    Flag of SwitzerlandSwitzerland
    Flag of United States of AmericaUnited States of America
    Flag of AustriaAustria

    Regulatory compliance

    EDQM
    GDUFA
    CE
    GMP
    JDMF
    KDMF
    FDA
    GDP
    NDC API
    USDMF
    CEP COS

    Audit standards

    GMP (Finished Dosage)

    Company description

    FAREVA stands as a prominent global pharmaceutical CDMO with leading expertise in the development and production of a wide variety of Drug Products and Active Pharmaceutical Ingredients (APIs). The company has a workforce of 13,000 individuals spread across 41 manufacturing facilities situated in 13 countries across EMEA and the Americas. Among these facilities, 18 are exclusively dedicated to pharmaceutical operations. FAREVA’s API division carries out its activities in 3 European locations situated in France and Germany.

  • Micro Labs

    Manufacturer
    Audited
    Audit report available
    Non-Compliance Report

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia

    Regulatory compliance

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

    Audit standards

    GMP (APIs)

    Company description

    We are a technology-focused, multi-dimensional pharmaceutical company having state-of-the-art manufacturing capabilities in diverse therapeutic areas such as Cardiology, Diabetology, Pain Management, Dermatology, Ophthalmology, Neurology and more. We strive towards unlocking the power of science to provide access to affordable and innovative medicines to improve health outcomes and make a difference in people's lives across the globe. As we continue to champion the cause of Make-in-India through our steady expansion across various Indian states, we create job opportunities and drive social responsibility programs in education, healthcare, rural development and environmental protection to add value to our local communities. Our roadmap is to continue investing in discovering, developing, manufacturing, and commercializing innovative medicines. Meeting the growth and profitability goals through successful innovation in digital healthcare trends and commercial excellence will continue to be the driving factors over the next decade.

  • 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 Granules India

    Granules India

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia

    Regulatory compliance

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

    Audit standards

    GMP (APIs)
    GMP (Finished Dosage)

    Company description

    Granules India Limited is a rapidly expanding pharmaceutical company with top-notch amenities for APIs, PFIs and Finished Dosages, catering to clients in more than 60 nations. We are dedicated to upholding high standards in production, excellence and client relations. Our main office is situated in Hyderabad, and we also have branches in the United States, United Kingdom, Colombia and China, as well as production facilities in India and China.

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