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New DMF awarded to Coster MDI valves – 20DR & 20DPH

  • Coster
  • Europe

  • Italy

  • Health

  • Pharmaceuticals

  • Primary Packaging

  • Aerosols

  • Aerosol Valves - Bag-on

  • Laboratory, Testing, Certification

  • National Certifications

  • FDA Approved

Europe, Italy, Health, Pharmaceuticals, Primary Packaging, Aerosols, Aerosol Valves - Bag-on, Laboratory, Testing, Certification, National Certifications, FDA Approved

Coherent with the strategy of consolidating its presence in the global Pharmaceutical domain, Coster has announced that the American FDA has recently awarded the company with a Type III Drug Master File (n. 26960) for its MDI valves: 20DR & 20DPH.

The valves are manufactured in Coster Trento (Italy) facility in a Clean Room Environment, Class 7 at rest.

The newly-awarded DMF joins another filed with the FDA in 2008 for BOVs (Bag-On-Valves) and series 1800 actuators, currently being used in association with anti-mycotic products among other applications.

For more information please send an e-mail to pharma@coster.com.

  • Company News
  • English
  • Modified 24 Aug 2015
  • Hits 2422