Pharmaceutical Printer of Inserts, Labels and More
Since 1928, we have been at the forefront of development in the pharmaceutical print industry. Beyond our reputation as the preeminent pharmaceutical printer, we now supply labeling and printing services for medical devices, as well as the bio-tech industry. We are committed to developing and then printing innovative materials that make it easier for you to get vital information to your customers. We do it all through a tried and tested foundation in Current Good Manufacturing Practices (CGMP) and ISO 9001:2015 standards that constantly work to achieve consistency in all of our print processes.
We are proud to boast that Pharmaceutic Litho is one of the few pharmaceutical printers with over 75,000 sq. ft. dedicated solely to pharmaceutical printing. Even so, we continue to grow and expand our secondary packaging services for the pharmaceutical and bio-tech industries in order to build on our reputation as the standard for quality and service in the pharma printing industries.
LATEST NEWS: Pharmaceutic Litho & Label Company Acquires Plymouth Printing
Wilton, CT — Pharmaceutic Litho & Label Company is excited to announce the acquisition of Plymouth Printing Company, Inc. As a current Good Manufacturing Practices (cGMP) compliant specialty printer that exclusively serves the pharmaceutical, biotech and medical device industries... continue reading
Pharmaceutical Printer Products
Pharmaceutical Inserts Outserts
Pharma Labels
Pharmaceutical Booklets
Pharmaceutical Manuals
Pharmaceutical Printer Services
Printing ♦ Labeling ♦ Biotech Labeling ♦ Medical Device Labeling ♦ Pharma Printing ♦ Secondary Packaging ♦ Lithography ♦ Flexography
years in print
loyal clients
annual orders
printed items each year
Pharmaceutical Printer News
Mylan Launches Generic Version Of The Novartis Exelon Patch
Mylan N.V. today announced the U.S. launch of Rivastigmine Transdermal System, 4.6 mg/24 hrs, 9.5 mg/24 hrs and 13.3 mg/24 hrs, a generic version of Novartis’ Exelon Patch. Mylan received final approval fromRead More…
FDA Approves Genentech’s Rituxan For Pemphigus Vulgaris
The U.S. Food and Drug Administration (FDA) has approved Genentech’s Rituxan (rituximab) for the treatment of adults with moderate to severe pemphigus vulgaris (PV), a rare, serious, potentially life-threatening condition characterized by progressive painfulRead More…
FDA Grants Priority Review of Genentech’s Tecentriq
Genentech, a member of the Roche Group today announced that the FDA has accepted the company’s supplemental Biologics License Application (sBLA) and granted Priority Review for Tecentriq (atezolizumab), in combination with Avastin (bevacizumab), paclitaxelRead More…