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Parteck® Functional Excipients

Tableting formulation

When you design a solid dosage form, there are many factors to consider: the active ingredient, bioavailability enhancement, release kinetics, specific dosage, packaging, shelf life, and more. Our Parteck® excipients were designed with the formulator’s challenges in mind and are particle optimized for excellent performance in formulation development and manufacture. Backed by the Emprove® program with its stringent quality control, as well as regulatory support and documentation, Parteck® excipients help to speed up your approval processes.

Flexible Tableting

  • High tablet hardness at low compression forces, providing tablet robustness and rapid disintegration
  • High and low API dosages enabled by the unique particle surface
  • Specialized excipients for direct compression, wet and dry granulation, film coating, lubrication, and rapid disintegration

Optimized Drug Delivery

  • Options for modifying release kinetics, such as orally disintegrating tablets and sustained-release solid oral formulations
  • Specialized excipients for different routes of administration, including dry powder inhalation

Enhanced Solubility

  • Specialized excipients that boost the efficacy of your final drug product by enhancing API solubility through the use of polyvinyl alcohol for hot melt extrusion, or a silica drug carrier with a unique surface structure

Related Product Resources

Flyer: Parteck® SLC Excipient for Enhanced Drug Solubility
Flyer: Parteck® M DPI Excipient for Dry Powder Inhalation
Flyer: Parteck® COAT Excipient for Reduced Coating Times
Flyer: Adapt to Succeed: Parteck® Delta M Excipient

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Related Product Categories
Solid Formulation
Our comprehensive portfolio of high-quality raw materials and functionalized excipients helps you meet the challenges of solid formulation pharmaceutical manufacturing, backed by regulatory support for simplified supplier qualification, accelerated processes, and reduced total cost of ownership.
Related Applications
Solid Formulation Strategies
Challenges such as API stability, release kinetics, and bioavailability have made the manufacturing of solid formulation pharmaceuticals more difficult, particularly given pressures to reduce costs and optimize process efficiency. Learn how new solutions and expert partnership can overcome these challenges.
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Emprove® Program
Confidently speed your way through the regulatory maze and fast track your new drug to market with the Emprove® Program. High-quality products, comprehensive documentation, and superior customer support facilitate your efforts in qualification, risk assessment, and process optimization.
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