Ferro Pfanstiehl Laboratories (FPL) has been a producer of proprietary and cGMP pharmaceutical ingredients for more than 35 years. We provide process development, analytical method development and validation, as well as Drug Master File creation and maintenance. FPL currently maintains more than 20 active Drug Master Files covering API's, intermediates and injectable drug formulation ingredients.

FPL has manufactured commercial quantities of potent and Cytotoxic API's for nearly two decades. Among our API's, FPL manufactures the Generic drugs Cytarabine and Streptozotocin. FLP contract manufactures several additional proprietary High Potency Anti-cancer and Anti-Viral drugs and advanced intermediates.

In 2000, FPL commissioned a state-of-the-art potent compound manufacturing facility that enables production of potent / highly toxic compounds in batches up to 50 Kilograms, using up to 300 gallon equipment.

Our customer list is a "Who's-Who" of multi-national pharmaceutical companies as well as small, medium, and virtual companies.

Under strict confidentiality, we will review your requirements and prepare a detailed development and/or product manufacturing quote. With early involvement in the clinical drug development process, we can help you move smoothly and quickly to market.

To explore a collaboration, contact us or call 1-800-383-0126. Ask us about make vs. buy options for your particular drugs or development project.