Key Milestones

  • 2004

    Established in Shenzhen, China

  • 2005

    Techdow's enoxaparin sodium injection (Prolongin®) became the first generic enoxaparin approved by China's National Medical Products Administration (NMPA, formerly CFDA)

  • 2010

    The enoxaparin sodium API production line passed the GMP inspections in China for the first time

  • 2012

    The enoxaparin sodium API production line passed the inspection by the U.S. Food and Drug Administration (FDA) for the first time

  • 2013

    Techdow's enoxaparin sodium API production line passed the inspection by Poland's Main Pharmaceutical Inspectorate (GIF) for the first time

  • 2015

    Techdow's enoxaparin sodium injection packaging line #1 passed the inspection by Poland's GIF for the first time

  • 2016

    Techdow's enoxaparin sodium injection syringe prefilling line #1 and vial production line passed the inspection by Poland's GIF for the first time

    Techdow's enoxaparin sodium prefilled syringe production line passed the GMP inspection in China for the first time

    Techdow's enoxaparin sodium injection (Inhixa/Neoparin) approved in the EU as the first enoxaparin biosimilar product in the region and the company began to build local sales teams for the 5 major European markets (Poland, Italy, United Kingdom, Germany, Spain)

  • 2018

    Acquired by Shenzhen Hepalink Pharmaceutical Group Co., Ltd., thus completed Hepalink's vertical integration of the entire heparin industrial chain with end-to-end coverage from APIs to heparin preparations

    Techdow's enoxaparin sodium PFS filling line #1 passed the inspection by the U.S. FDA for the first time

  • 2019

    Techdow's enoxaparin sodium vial bottling line passed the inspection by the U.S. FDA for the first time

    Techdow's enoxaparin sodium PFS filling line #2 and packaging line #3 passed the inspection by Poland's GIF for the first time

  • 2020

    All SKUs of enoxaparin sodium injection (Prolongin®) marketed in China passed the Bioavailability Equivalence Evaluation of the Quality and Efficacy of Biosimilar, and became the first product that passed the evaluation in China at the time

  • 2021

    Established Techdow USA and began building a local sales team in the U.S.

    Techdow's enoxaparin sodium PFS filling line #2 passed the inspection by Poland's GIF for the first time

  • 2022

    Officially began selling heparin sodium injections in the U.S.

  • 2023

    The company’s enoxaparin sodium injection product (product name: Enoxaparin Sodium Injection, USP) was approved by the U.S. Food and Drug Administration (FDA) and subsequently launched in the U.S. market

    Techdow's enoxaparin sodium injection (Prolongin®) became the first enoxaparin product selected by the 8th Centralized National Procurement in China

Legal statement   ·   Environmental Disclosure

Copyright ©2022 Shenzhen Techdow Pharmaceutical Co., Ltd