Risedronate sodium 2.5-hydrate

Risedronate sodium 2.5-hydrate
Product Description

Risedronate is used to treat osteoporosis caused by menopause, or steroid use. risedronate is for use when you have a high risk of bone fracture due to osteoporosis. Risedronate is also used to treat Paget's disease of bone. Risedronate may also be used for purposes not listed in this medication guide.

Polpharma API

  • Long experience in in-house commercial manufacturing
  • Extensive portfolio of Bisphosphonates
  • Technology not generating genotoxic impurities

  • Polpharma S.A.

    • PL
    • 2015
      On CPHI since
    • 4
      Certificates
    • 5000+
      Employees
    Company types
    CMO/CDMO
    Contract Service
    Generics/Biosimilars Manufacturer
    Manufacturer/Innovator
    Pharmaceutical company
    Specifications
    • CAS Registry Number
      329003-65-8
    • Details
      Status Commercial


      Therapeutic cat. Musculo-skeletal


      Polymorphic formForm A


      CAS No.329003-65-8


      Injectable Form


      EU DMF readiness


      CEP


      JAPANESE DMF


      KOREAN  DMF


      CANADIAN  DMF


      CADIFA -pending


      US DMF readiness
    • Selling Points
      ✔️ HP API (OEL up to 10 ng/m3)
      ✔️ EU manufacturing site
      ✔️ US FDA-approved
      ✔️ 70 years of experience in small molecules
      ✔️ cGMP manufacturing
      ✔️ Highest quality standards
      ✔️ Research, Development, and Commercial Manufacturing
      ✔️ World-class regulatory support
      ✔️ Smooth and transparent cooperation

    Polpharma S.A.

    • PL
    • 2015
      On CPHI since
    • 4
      Certificates
    • 5000+
      Employees
    Company types
    CMO/CDMO
    Contract Service
    Generics/Biosimilars Manufacturer
    Manufacturer/Innovator
    Pharmaceutical company

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    Polpharma S.A. resources (5)

    • News CPHI Barcelona 2023: Tackling the Pharma Talent Precipice – Part 2

      This year at CPHI Barcelona (24–26 October, 2023) we sat down with C-suite executives and HR professionals to discuss the looming talent crisis in the pharmaceutical industry. With hybrid working persisting post-pandemic and a growing skills gap, how can the pharmaceutical supply chain adjust to a changing labour force? 
    • Brochure API Product List 2025

      Thanks to over 70 years of experience in process development, scale-up and cGMP manufacturing, we support both emerging and established pharmaceutical customers in the development and commercialization of their small molecule API clinical candidates. At our FDA-approved plant located in Central Europe, we provide end-to-end solutions from API development to scale-up allowing smooth process transfer for commercial-scale manufacturing capabilities, with world-class regulatory support. Our strong R&D management team, experienced in the development of chemical processes and complex projects, provides a wide range of solutions to our customers, applying a variety of chemical reactions and conditions, including cryogenic, High Pressure, strong base reactions, and tailor-made particle size distribution modifications. At Polpharma quality comes first. Regular FDA audits prove our reliability and credibility towards business partners around the world.
    • News KiloLab Laboratory: strategic milestone achieved!

      KiloLab Laboratory – a development and production in a kilogram scale – has been launched, according to Polpharma API development strategy adopted in 2021.
    • Brochure Polpharma API CDMO offer

      Thanks to over 70 years of experience in process development, scale-up and cGMP manufacturing, we support both emerging and established pharmaceutical customers in the development and commercialization of their small molecule API clinical candidates. At our FDA-approved plant located in Central Europe, we provide end-to-end solutions from API development to scale-up allowing smooth process transfer for commercial-scale manufacturing capabilities, with world-class regulatory support. Our strong R&D management team, experienced in the development of chemical processes and complex projects, provides a wide range of solutions to our customers, applying a variety of chemical reactions and conditions, including cryogenic, High Pressure, strong base reactions, and tailor-made particle size distribution modifications. At Polpharma quality comes first. Regular FDA audits prove our reliability and credibility towards business partners around the world.
    • Video Strategic investment HP API facility

      As an EU-based Contract Development and Manufacturing Organization (CDMO) and supplier of active pharmaceutical ingredients, we are advancing our technology capabilities with an Occupational Exposure Limit (OEL) as low as 10 ng/m³ (OEB 6).
      Our new capabilities enable GMP and FDA-approved kilo-scale production, offering batch sizes of up to 1.5 kg. This facility features dedicated Analytical Development Laboratories (ADL) and Process Development Laboratories (PDL) to ensure comprehensive support for all production phases. The design incorporates state-of-the-art isolator technology to ensure the safety of both personnel and products, along with industry-standard secondary containment solutions integrated into the infrastructure.
      We have secured future capacity expansion through both internal enhancements and external partnerships, with the goal of doubling our production capacity.

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