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    Pharmaceutical manufacturers of Morphine sulfate

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

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    18results for pharmaceutical manufacturers of Morphine sulfate

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    • Small logo of Hameln rds

      Hameln rds

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of SlovakiaSlovakia

      Sites

      Flag of SlovakiaSlovakia

      Regulatory compliance

      EDQM
      KDMF
      GDP
      CEP COS

      Audit standards

      GMP (APIs)
      GMP (Subcontracted Laboratory)

      Company description

      Hameln rds s.r.o. is situated in Slovakia, a member of the European Union, in the region of Europe. It is a reputable pharmaceutical company that specializes in producing APIs and providing services for the healthcare sector, focusing on various stages of pharmaceutical product development and production, encompassing analytical and galenical development. Hameln offers a broad spectrum of services, including QC services (such as stabilities and batch release) and the development and manufacturing of APIs. Serving as a centralized API production facility, supply and trading chain, as well as a hub for research and development, Hameln rds plays a pivotal role in the pharmaceutical industry.

    • Small logo of Catalent

      Catalent

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of United States of AmericaUnited States of America

      Sites

      Flag of ItalyItaly
      Flag of JapanJapan
      Flag of BelgiumBelgium
      Flag of FranceFrance
      Flag of United KingdomUnited Kingdom
      Flag of United States of AmericaUnited States of America
      Flag of ArgentinaArgentina
      Flag of GermanyGermany
      Flag of CanadaCanada
      Flag of AustraliaAustralia
      Flag of Puerto RicoPuerto Rico

      Regulatory compliance

      EDQM
      GDUFA
      JDMF
      FDA
      NDC API
      USDMF

      Audit standards

      GMP (Finished Dosage)

      Company description

      Catalent is the global leader in enabling pharma, biotech, and consumer health partners to optimize product development, launch, and full life-cycle supply for patients around the world. With broad, deep-scale and expertise in development sciences, delivery technologies, and multi-modality manufacturing, Catalent is a preferred Contract Development and Manufacturing Organization (CDMO) partner for personalized medicines, blockbuster drugs and consumer health brand extensions. Catalent helps accelerate over 1,000 partner programs and launch over 150 new products every year. Its flexible manufacturing platforms at over 50 global sites supply over 80 billion doses of nearly 8,000 products annually. Its rapidly growing expert workforce exceeds 18,000, including more than 3,000 scientists and technicians. Headquartered in Somerset, New Jersey, Catalent, Inc. (NYSE:CTLT), is in S&P 500® company, and generated nearly $5 billion in revenue in its 2022 fiscal year.

    • Small logo of Euroapi

      Euroapi

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of FranceFrance

      Sites

      Flag of FranceFrance
      Flag of HungaryHungary
      Flag of GermanyGermany
      Flag of United KingdomUnited Kingdom
      Flag of ItalyItaly
      Flag of SlovakiaSlovakia

      Regulatory compliance

      EDQM
      GDUFA
      KDMF
      JDMF
      FDA
      CEP COS
      USDMF
      NDC API

      Audit standards

      GMP (APIs)

      Company description

      Euroapi focuses on revolutionizing active component solutions to sustainably fulfill the demands of clients and patients globally. As a prominent figure in active pharmaceutical ingredients, we possess a comprehensive portfolio of around 200 products, encompassing a wide range of technologies, and are constantly developing innovative molecules through our Contract Development and Manufacturing Organization (CDMO). Our 3,350 employees are driven by the commitment to improving access to essential therapies and promoting health

    • Small logo of Siegfried

      Siegfried

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of SwitzerlandSwitzerland

      Sites

      Flag of ArgentinaArgentina
      Flag of GermanyGermany
      Flag of FranceFrance
      Flag of United States of AmericaUnited States of America
      Flag of SwitzerlandSwitzerland
      Flag of MaltaMalta
      Flag of People's Republic of ChinaPeople's Republic of China

      Regulatory compliance

      GMP
      JDMF
      KDMF
      EDQM
      FDA
      GDUFA
      USDMF
      CEP COS
      NDC API

      Audit standards

      GMP (Finished Dosage)
      GMP (APIs)

      Company description

      Siegfried serves as your favored associate for comprehensive integrated pharmaceutical ingredient and drug product services with manufacturing capabilities globally. Our expertise is crucial for your venture throughout the entire lifespan. Our enthusiasm lies in creating and producing formulations. It is extraordinary for a provider of development and manufacturing services to possess such a blend of inherent technical expertise and knowledge. Pharmaceutical ingredient services entail Tailored Development and Outsourced Manufacturing for both active pharmaceutical ingredients (API) and intermediates, along with our own range of API (opiates and other regulated substances) and documentation featuring independent patented technologies. Clients utilizing our drug product services benefit from a wealth of inherited expertise in intricate oral drug delivery systems, including sterile filling, backed by in-house development, customer development and manufacturing, and a wide array of completed dosage form products. Enhancing chemical processes and formulations is our area of specialization. We collaborate closely with clients to innovate and enhance chemical processes, thus providing additional benefits and value. Siegfried operates at 11 locations globally, spanning both the Eastern and Western Hemispheres, with multi-purpose cGMP chemical manufacturing facilities in Zofingen, Switzerland; Pennsville, New Jersey, USA; Nantong, China; Minden, Germany; Saint-Vulbas, France; Evionnaz, Switzerland; and sites for manufacturing drug products in Zofingen, Switzerland; Malta; Hameln, Germany, Irvine, USA; Barberà del Vallès, Spain and El Masnou, Spain. Count on Siegfried as your preferred partner for more opportunities.

    • 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 Mallinckrodt Pharmaceuticals

      Mallinckrodt Pharmaceuticals

      Manufacturer

      Headquarters

      Flag of United KingdomUnited Kingdom

      Sites

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

      Regulatory compliance

      JDMF
      KDMF
      GDP
      USDMF
      NDC API
      CEP COS

      Company description

      MNK’s Specialty Generics division provides a wide variety of high-quality generic medications, focusing on pain relief, addiction treatment, and ADHD, as well as a comprehensive range of active pharmaceutical ingredients (APIs), such as acetaminophen/paracetamol, DEA scheduled compounds, and stearates. We run the largest API facility in the United States. Discover the range of excipients available from Mallinckrodt Pharmaceuticals for use in pharmaceutical drug delivery systems (DDS).

    • Small logo of Saneca Pharmaceuticals

      Saneca Pharmaceuticals

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of SlovakiaSlovakia

      Sites

      Flag of SlovakiaSlovakia
      Flag of TürkiyeTürkiye

      Regulatory compliance

      JDMF
      KDMF
      GDP
      EDQM
      CEP COS
      USDMF
      NDC API

      Audit standards

      GMP (Finished Dosage)
      GMP (APIs)

      Company description

      We are the largest pharmaceutical company in Slovakia with site originally established in the 1940s. Our multi-purpose headquarters is easily reachable from all central European hubs like Vienna, Prague and Budapest. We, at Saneca, are proud of our tradition and reputation. We help improve the quality of life.

    • Small logo of Temad

      Temad

      Manufacturer

      Headquarters

      Flag of Islamic Republic of IranIslamic Republic of Iran

      Sites

      Flag of Islamic Republic of IranIslamic Republic of Iran

      Regulatory compliance

      EU WC
      JDMF

      Company description

      Established in 1997, Temad Co. has been operating for over two decades and is recognized as one of the leading manufacturers of APIs in Iran. It is also known for its groundbreaking production of both narcotic and non-narcotic products with exceptional quality within the Middle East. In addition to adhering to Iranian GMP regulations, Temad has met the national and international standards of API manufacturing, including ISO 9001/14001/17025/45001 and OHSAS 18001. With a portfolio of over 115 pharmaceutical products, Temad ensures compliance with GMP and WHO standards as well as regulations for both narcotic and non-narcotic medications. The company proudly exports its diverse range of products to 45 countries across the globe.

    • 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
    • Small logo of Pluviaendo

      Pluviaendo

      Manufacturer

      Headquarters

      Flag of TürkiyeTürkiye

      Sites

      Flag of NetherlandsNetherlands

      Regulatory compliance

      FDA
      EDQM

      Company description

      Pluvia Consumer Health operates as a multinational pharmaceutical firm and is headquartered in Istanbul, Turkey. The company possesses unique molecules and expertise. Its product portfolio comprises distinct APIs and Finished Dosage Form medications focusing on opioid medications, cosmeceuticals, and nutraceutical supplements, all supported by modern processing systems. The company's ability to manufacture its products in-house, leveraging its proprietary know-how from A to Z, enables it to provide comprehensive support in documentation, formulation, and scientific matters, as well as supply high-quality products at unbeatable prices, covering various types of APIs.

    • Small logo of SALARS SpA

      SALARS SpA

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of ItalyItaly

      Sites

      Flag of ItalyItaly
      Flag of AustraliaAustralia

      Regulatory compliance

      KDMF
      USDMF
      CEP COS
      NDC API

      Audit standards

      GMP (APIs)

      Company description

      Founded in 1932 in Milan, it was the first company authorised to process opiates for the pharmaceutical industry. Even today it is the only manufacturing company (authorized to produce narcotic substances) existing in our country. Our goal is to produce active pharmaceutical ingredients respecting the highest quality standards aimed at pain therapy. At every stage of the production process we strive to optimize resources, maintain a high level of quality and follow the indications dictated by the regulations in force.

    • Small logo of Wood & Financial Services

      Wood & Financial Services

      Manufacturer

      Sites

      Flag of SlovakiaSlovakia

      Regulatory compliance

      EDQM
      CEP COS
      KDMF
      USDMF
      NDC API
      JDMF
    • Verve Human Care Laboratories

      Manufacturer

      Headquarters

      Flag of IndiaIndia

      Sites

      Flag of IndiaIndia

      Regulatory compliance

      WHO GMP

      Company description

      Verve Human Care Laboratories is the premier Pharmaceutical Finished Formulation Manufacturer and Exporter in the field of analgesics and anesthesia in India. Specializing in Narcotic and Psychotropic Products, our production facility adheres to the standards set by US-FDA and PIC/S guidelines. Our current approvals include WHO-GMP, TFDA-Tanzania, PMPB-Malawi, FDA Ghana, PPB-Kenya, NDA-Uganda, FMHACA-Ethiopia, SFDA-Saudi Arabia, MOH-Cambodia, MCAZ-Zimbabwe with ongoing approval processes in many other countries.

    • Small logo of Alkermes

      Alkermes

      Manufacturer
      Warning letter

      Headquarters

      Flag of IrelandIreland

      Sites

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

      Regulatory compliance

      KDMF
      JDMF
      FDA
      EDQM
      NDC API
      USDMF
    • Aradigm

      Manufacturer

      Headquarters

      Flag of United States of AmericaUnited States of America

      Regulatory compliance

      USDMF

      Company description

      Aradigm is actively involved in fulfilling the commitment to developing inhalation medication products that could potentially transform the quality of life for patients with severe pulmonary conditions. Since 1991, the organization has assembled an exceptional group of researchers, technicians, and medical specialists who have been leading the way in the creation of innovative inhalation delivery products. This team, for instance, spearheaded the AERx® pulmonary delivery platform, which underwent testing in numerous patients using various medications and biologics such as insulin, fentanyl, erythropoietin, and nicotine.

    • Cody Laboratories

      Manufacturer

      Headquarters

      Flag of United States of AmericaUnited States of America

      Sites

      Flag of United States of AmericaUnited States of America

      Regulatory compliance

      FDA
      GDUFA
      USDMF
    • Small logo of Alcaliber

      Alcaliber

      Manufacturer
      Audited
      Audit report available

      Headquarters

      Flag of SpainSpain

      Sites

      Flag of SpainSpain

      Regulatory compliance

      KDMF
      CEP COS

      Audit standards

      GMP (APIs)
    • Paion

      Manufacturer

      Headquarters

      Flag of United KingdomUnited Kingdom

      Regulatory compliance

      USDMF
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