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    Pharmaceutical manufacturers of Lisdexamfetamine

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

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    10results for pharmaceutical manufacturers of Lisdexamfetamine

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    • Small logo of Ind Swift Laboratories

      Ind Swift Laboratories

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of IndiaIndia

      Sites

      Flag of IndiaIndia
      Flag of ItalyItaly

      Regulatory compliance

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

      Audit standards

      GMP (APIs)

      Company description

      Headquartered in Chandigarh, India, Ind-Swift Laboratories Ltd. today is a global manufacturer of APIs, Intermediates, and formulations (through group collaboration). With regulated 6+ manufacturing sites (including 2 group subsidiaries) in Punjab and Jammu, we cater to the API needs of regulated markets including USFDA, EDQM, PMDA, ANVISA, EU-GMP, KFDA, NMO, ANSM, Cofepris, TGA, WHO, ROW. Today, Ind-Swift Laboratories Ltd. is a significant player in manufacturing APIs towards Cardiovascular health, Antihistamine, Antidiabetic, Antipsychotic, Antimigraine, Parkinson’s Disease, Antineoplastic, ADHD Symptoms, Analgesics, Alcohol Abstinence and Bone Resorption Inhibitor. We also hold global leadership positions in the Macrolide Antibiotic segment.

    • 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 Veranova

      Veranova

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of United States of AmericaUnited States of America

      Sites

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

      Regulatory compliance

      EDQM
      GDUFA
      GMP
      KDMF
      FDA
      JDMF
      USDMF
      NDC API
      CEP COS

      Audit standards

      GMP (APIs)

      Company description

      Veranova boasts over 50 years of expertise and is a frontrunner in the creation and fabrication of intricate and specialized APIs for the pharmaceutical and biotech sectors. It was previously a segment of Johnson Matthey, specializing in intricate and regulated chemical processes. The company delivers customized services throughout all phases of drug development and is split into Generics and Originators. It possesses a variety of development technologies and areas of expertise, along with a cooperative approach to API manufacturing and procedures.

    • Small logo of Alkem Laboratories

      Alkem Laboratories

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of IndiaIndia

      Sites

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

      Regulatory compliance

      EDQM
      WHO GMP
      KDMF
      EU WC
      FDA
      GDUFA
      GDP
      USDMF

      Audit standards

      GMP (APIs)

      Company description

      Established in 1973 and based in Mumbai, India, Alkem started its operations as a healthcare marketing firm. Alkem is a major participant in the market for branded and generic drugs in India. The company has a strong presence in various therapeutic segments such as Anti-infective, Gastro-intestinal, Pain Management, Vitamins/Minerals/Nutritions, Central Nervous System, Anti-diabetic, Anti-osteoporosis, Anti-malarial, Cardiovascular, Immunosuppressants, and Nutraceutical segment.

    • Small logo of Archimica

      Archimica

      Manufacturer
      Audited

      Headquarters

      Flag of ItalyItaly

      Sites

      Flag of ItalyItaly

      Regulatory compliance

      FDA
      JDMF
      KDMF
      GDUFA
      USDMF
      NDC API
      CEP COS

      Audit standards

      GMP (APIs)

      Company description

      Our proprietary products (APIs) cater to the general pharmaceutical sector. We consistently deliver high-quality products and services, utilizing some of the most challenging chemical technologies in the world responsibly and continuously

    • 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 Embio

      Embio

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of IndiaIndia

      Sites

      Flag of IndiaIndia

      Regulatory compliance

      EU WC
      JDMF
      KDMF
      GDUFA
      FDA
      USDMF
      NDC API
      CEP COS

      Audit standards

      GMP (APIs)

      Company description

      Technology and innovation is the backbone of Embio’s success, which allows us to achieve a leadership position as a manufacturer of Active Pharmaceutical Ingredients (APIs), Intermediates and Speciality chemicals catering to a range of global customers in the pharmaceutical, nutraceutical, food, cosmetic, crop & plant protection segments. With 30+ years of experience in handling bacterial, fungal & Category 1 GMO bio-transformation, Embio has demonstrated an impeccable track record in creating sustainable, environmental friendly and disruptive technologies. With licenses to manufacture Schedule-1 & Schedule-2 substances, Embio is a leading global player in the domain of controlled substances, advanced intermediates & chiral molecules. Embio’s State of the Art manufacturing facility is approved by US-FDA, PMDA, KFDA, COFEPRIS & WHO-GMP. Our products & services cater to the stringent requirements of a large customer base in more than 70 countries, with a major share from regulated markets that includes originator and large multi-national companies.

    • Small logo of Chr. Olesen

      Chr. Olesen

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of DenmarkDenmark

      Sites

      Flag of GermanyGermany
      Flag of DenmarkDenmark

      Regulatory compliance

      EDQM
      GDP
      CEP COS
      USDMF

      Audit standards

      GDP (Distribution)
      GMP (APIs)
      GMP (Starting Materials)

      Company description

      Chr. Olesen Group operates as a global consortium of partner-led distribution and production firms. Chr. Olesen focuses on distributing ingredients and API’s across four distinct sectors: Feed, Food, Pharma, and Vet Pharma. The manufacturing arm of the group, Chr. Olesen Synthesis, is headquartered in Denmark and specializes in API's and intermediates, with particular emphasis on controlled substances such as Buprenorphine HCL, Buprenorphine base, and Buprenorphine intermediates, along with Dexamphetamine sulphate, Hydromorphone, Terbinafine, and Tolfenamic acid. Established in 1885, Chr. Olesen Group is presently under the management of the fourth generation.

    • Small logo of Noramco

      Noramco

      Manufacturer
      Audited

      Headquarters

      Flag of United States of AmericaUnited States of America

      Sites

      Flag of United States of AmericaUnited States of America

      Regulatory compliance

      KDMF
      FDA
      GDUFA
      NDC API
      USDMF
      CEP COS
    • Chattem Chemicals

      Manufacturer

      Headquarters

      Flag of United States of AmericaUnited States of America

      Sites

      Flag of United States of AmericaUnited States of America

      Regulatory compliance

      KDMF
      FDA
      GDUFA
      USDMF
      NDC API
      CEP COS
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    Some information included may be sourced from the European Medicines Agency website (https://www.ema.europa.eu/) or the U.S. Food & Drug administration website (https://www.fda.gov/). Please note that Qualifyze does not guarantee the completeness or timeliness of the content. Qualifyze is not liable for any inaccuracies, errors or omissions in the content sourced from such sources.

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