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  1. Supplier directory
  2. Pharmaceutical manufacturers
  3. Metoprolol tartrate

Pharmaceutical manufacturers of Metoprolol tartrate

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

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28results for pharmaceutical manufacturers of Metoprolol tartrate

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  • Pliva Hrvatska

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of CroatiaCroatia

    Sites

    Flag of CroatiaCroatia
    Flag of United States of AmericaUnited States of America
    Flag of PolandPoland
    Flag of IndiaIndia
    Flag of Czech RepublicCzech Republic

    Regulatory compliance

    FDA
    JDMF
    KDMF
    GDUFA
    NDC API
    CEP COS
    USDMF

    Audit standards

    GMP (APIs)
    GMP (Finished Dosage)

    Company description

    We are committed to providing innovative and quality medicines to the nearly 200 million people we serve around the world every day; we make contact with patients, families and communities for better health and better days.

  • 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 Sicor

    Sicor

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of ItalyItaly

    Sites

    Flag of ItalyItaly
    Flag of MexicoMexico
    Flag of GermanyGermany
    Flag of LithuaniaLithuania
    Flag of United States of AmericaUnited States of America

    Regulatory compliance

    JDMF
    KDMF
    FDA
    GDUFA
    NDC API
    USDMF
    CEP COS

    Audit standards

    GMP (APIs)

    Company description

    Sicor, situated in the northern region of Italy, is a component of the Teva API business and offers a worldwide platform for the production and promotion of APIs for injectable, inhalation, topical, and nasal products. These specialized facilities possess a significant level of skill, manufacturing approximately 60 active pharmaceutical ingredients.

  • Small logo of Esteve Quimica

    Esteve Quimica

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of SpainSpain

    Sites

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

    Regulatory compliance

    GMP
    EDQM
    KDMF
    JDMF
    FDA
    GDUFA
    USDMF
    CEP COS
    NDC API

    Audit standards

    GMP (APIs)

    Company description

    At Esteve Quimica, we are dedicated to the healthcare sector by providing support for the advancement and commercialization of products that enhance the health of patients. Established in 1966, our company remains privately owned despite being a part of ESTEVE, one of the largest pharmaceutical groups in Spain. Our current focus is on the development and production of small molecule intermediates and active ingredients for innovator companies, operating as a dedicated third-party contract business.

  • Small logo of Erregierre

    Erregierre

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of ItalyItaly

    Sites

    Flag of ItalyItaly

    Regulatory compliance

    KDMF
    JDMF
    GDUFA
    FDA
    EDQM
    USDMF
    CEP COS
    NDC API

    Audit standards

    GMP (APIs)

    Company description

    Erregierre, with its two manufacturing facilities, one situated in San Paolo D'Argon (Bergamo) and the other in Sovere (Bergamo), is a privately owned independent company from Italy established in 1974. It is a leading producer of pharmaceutical active components created through synthesis and distributed globally. Erregierre has undergone inspection by the FDA and is deeply dedicated to manufacturing in strict compliance with cGMPs and the highest global quality standards.

  • 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 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.

  • Microsin

    Manufacturer
    Audited

    Headquarters

    Flag of RomaniaRomania

    Sites

    Flag of RomaniaRomania

    Regulatory compliance

    CEP COS
  • Small logo of Kopran

    Kopran

    Manufacturer
    Audited

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia

    Regulatory compliance

    KDMF
    EU WC
    EDQM
    USDMF
    CEP COS
    NDC API

    Company description

    Kopran Ltd is a globally operating pharmaceutical company focused on marketing and production. The company possesses two WHO GMP approved manufacturing facilities. Their FDF facility in Khopoli is accredited by TGA, MHRA, and MCC, while their API facility in Mahad holds WHO GMP accreditation. Kopran Ltd exports its products to prominent markets in Europe, Southeast Asia, and Latin America. The company offers a diverse range of Active Pharmaceutical Ingredients (APIs) in categories such as Anti-hypertensive, Macrolides, Neuromodulator, Cephalosporins, Carbapenems, and Oncology, as well as Finished Dosage Forms in Carbapenems, Gastroenterology, Anthelmintics, Central Nervous System, Pain management, Anti-allergies, Anti-asthmatics, Anti-Infectives, Penicillins, Cardiovascular, Antiprotozoal, Oncology, Anti-Diabetics, Erectile Dysfunction, and Macrolides.

  • Small logo of Sun Pharmaceutical Industries

    Sun Pharmaceutical Industries

    Manufacturer
    Audited
    Audit report available
    Warning letter

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of AustraliaAustralia
    Flag of IndiaIndia
    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.

  • Actavis

    Manufacturer
    Audited
    Audit report available
    Warning letter

    Headquarters

    Flag of IrelandIreland

    Sites

    Flag of United States of AmericaUnited States of America
    Flag of ItalyItaly
    Flag of IndiaIndia
    Flag of MaltaMalta
    Flag of United KingdomUnited Kingdom
    Flag of ArgentinaArgentina
    Flag of TürkiyeTürkiye
    Flag of BrazilBrazil
    Flag of MexicoMexico
    Flag of TaiwanTaiwan
    Flag of UruguayUruguay
    Flag of IrelandIreland
    Flag of BulgariaBulgaria
    Flag of RomaniaRomania
    Flag of Puerto RicoPuerto Rico

    Regulatory compliance

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

    Audit standards

    GMP (Finished Dosage)
  • 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 Emcure Pharmaceuticals

    Emcure Pharmaceuticals

    Manufacturer
    Warning letter

    Headquarters

    Flag of IndiaIndia

    Sites

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

    Regulatory compliance

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

    Company description

    Emcure Pharmaceuticals is driven by the purpose to develop, manufacture and market a broad range of pharmaceutical products globally. Our core strength and competitive advantage lie in our established presence in all major therapeutic areas including Gynaecology, cardiology, blood-related, oncology, respiratory, CNS & HIV among others. Emcure has launched 6 Biologics in the Domestic Market & RoW markets & they are the domestic leader in three biologics. With 350+ brands, five R&D centers and 13 manufacturing facilities established across the country, we have ensured a strong presence not just in India but also outside India with a wide network across 70+ countries. Our API facilities ensures that our supply chain is vertically integrated providing flexibility over control of manufacturing. We have cemented strategic global partnerships that are a result of alliances with local and multi-national companies which are at the helm of leadership in key therapeutic areas. The key objective of our widespread presence across markets is to constantly innovate and deliver affordable & high-quality healthcare solutions to people.

  • Small logo of Ctx Lifesciences

    Ctx Lifesciences

    Manufacturer
    Audited
    Warning letter

    Headquarters

    Flag of IndiaIndia

    Sites

    Flag of IndiaIndia

    Regulatory compliance

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

    Company description

    CTX is a rapidly expanding Indian manufacturer of APIs and Intermediates, conducting operations across 70 nations. Over the past five years, the focus has been on elevating the organization by unwaveringly serving the pharmaceutical industry. CTX holds accreditations from US FDA, EU GMP, PMDA Japan, and COFEPRIS Mexico cGMP. The core business approach of CTX Life Sciences is to become a global pharmaceutical and chemical industry partner while ensuring consistent supply of APIs and Intermediates, along with DMF, CEP, Written Confirmations, FDF, Prices, Patents, Patents & Exclusivities, Dossier, Manufacturer, Licensing, Distributer, Suppliers, News, and GMP Xlife Sciences.

  • Apeloa Pharmaceutical

    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

    Regulatory compliance

    EDQM
    KDMF
    FDA
    GDUFA
    NDC API
    JDMF
    USDMF
    CEP COS

    Audit standards

    GMP (APIs)

    Company description

    Apeloa Pharmaceutical Co., Ltd. is a major high-tech enterprise at the state level and a significant player in the pharmaceutical industry in Zhejiang Province. Our company focuses on the exploration, production, and marketing of pharmaceutical goods, primarily specializing in crude drug (API), contract R & D, production service (CDMO), and preparation (FDF) operations. Our product range is predominantly focused on cardio-cerebrovascular, anti-infection, anti-tumor, and other medical treatment areas. Currently, we produce over 70 types of raw materials on a large scale, with 11 of them exceeding 100 million in sales.

  • Small logo of Cosma

    Cosma

    Manufacturer
    Audited
    Audit report available

    Headquarters

    Flag of ItalyItaly

    Sites

    Flag of ItalyItaly

    Regulatory compliance

    GDUFA
    JDMF
    KDMF
    FDA
    USDMF
    NDC API
    CEP COS

    Audit standards

    GMP (APIs)

    Company description

    COSMA S. P. A. (established in 1977) and AMSA S. P. A. (established in 1953) are a pair of chemical facilities widely recognized globally and particularly valued in the occidental world and in the nations that adhere to the Pharmaceutical Inspection Convention (PIC). They are part of the CFM Group, a privately-owned company engaged in the fields of chemistry and pharmaceuticals since 1949

  • Small logo of Recordati

    Recordati

    Manufacturer
    Audited

    Headquarters

    Flag of ItalyItaly

    Sites

    Flag of ItalyItaly
    Flag of TürkiyeTürkiye

    Regulatory compliance

    GDUFA
    JDMF
    FDA
    GDP
    CEP COS
    NDC API
    USDMF

    Company description

    Recordati, an Italian pharmaceutical company, is publicly traded on the Italian Stock Exchange. Its unique structure allows it to provide healthcare solutions in various areas including specialty and primary care, consumer healthcare, and rare diseases. With a history dating back to 1926, Recordati has a presence in around 150 countries spanning the EMEA, Americas, and APAC regions.

  • Small logo of S.I.M.S.

    S.I.M.S.

    Manufacturer
    Audited

    Headquarters

    Flag of ItalyItaly

    Sites

    Flag of ItalyItaly

    Regulatory compliance

    FDA
    GDUFA

    Company description

    Società Italiana Medicinali Scandicci, known as S.I.M.S. srl, was established in Scandicci in 1937 by Mr Ugo Rangoni. During the 1950s and 1960s, it experienced growth in both production and personnel. In 1972, the first DMF (phenylbutazone) was presented to the FDA. The current API facility in Reggello has been operational since 1974 and has been regularly examined by the Agency ever since. Since the 1980s, the company has garnered increasing recognition in the field of custom-toll manufacturing through GMP status with major partners. The company has more than 20 APIs with registered DMF and, when applicable, the corresponding CEP.

  • Ra Chem Pharma

    Manufacturer

    Sites

    Flag of IndiaIndia

    Regulatory compliance

    EDQM
    EU WC
    GDUFA
    KDMF
    FDA
    USDMF
    NDC API
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