MedPath

PKU HealthCare Corp., Ltd.

PKU HealthCare Corp., Ltd. logo
🇨🇳China
Ownership
Public, Subsidiary
Established
1993-05-18
Employees
578
Market Cap
-
Website
http://www.pku-hc.com
Introduction

The company's predecessor was Southwest Synthetic Pharmaceutical Factory, founded in 1965, and successfully listed on the Shenzhen Stock Exchange in 1997. The company has built a nationwide pharmaceutical sales network covering everything from drug sales, pharmaceutical distribution, hospital collection to supply chain hosting. In the future, the company will strive to build a nationally leading generic pharmaceutical technology enterprise integrating raw materials and formulations, and become a pharmaceutical listed company with an important influence in the Chinese pharmaceutical industry. The company is mainly engaged in R&D, production and sales of chemical preparations, pharmaceutical distribution, and medical services. The company's main products: injectable ceftriaxone, meropenem for injection, cefaminol sodium hydrochloride, clindamycin palmitate granules, buspirone hydrochloride tablets, naphthymidone capsules, celecoxib capsules, dexketoprofen tablets, dexketoprofen capsules, buspirone hydrochloride tablets, olanzapine tablets. Corporate honors: A national technology center, a key Chinese pharmaceutical enterprise, a national innovative pilot enterprise, a key high-tech enterprise of the National Torch Program, etc.

Clinical Trials

0

Active:0
Completed:0

Trial Phases

0 Phases

Drug Approvals

175

NMPA:175

Drug Approvals

Buspirone Hydrochloride Tablets

Product Name
奇比特
Approval Number
国药准字H20247318
Approval Date
Dec 16, 2024
NMPA

Vortioxetine Hydrobromide Tablets

Product Name
氢溴酸伏硫西汀片
Approval Number
国药准字H20249357
Approval Date
Nov 15, 2024
NMPA

Quetiapine Fumarate Extended-Release Tablets

Product Name
富马酸喹硫平缓释片
Approval Number
国药准字H20249352
Approval Date
Nov 15, 2024
NMPA

Vortioxetine Hydrobromide Tablets

Product Name
氢溴酸伏硫西汀片
Approval Number
国药准字H20249358
Approval Date
Nov 15, 2024
NMPA

Vortioxetine Hydrobromide Tablets

Product Name
氢溴酸伏硫西汀片
Approval Number
国药准字H20249356
Approval Date
Nov 15, 2024
NMPA

Paroxetine Hydrochloride Enteric-Coated Sustained-Release Tablets

Product Name
盐酸帕罗西汀肠溶缓释片
Approval Number
国药准字H20249181
Approval Date
Oct 22, 2024
NMPA

Oseltamivir Phosphate For Suspension

Product Name
磷酸奥司他韦干混悬剂
Approval Number
国药准字H20244903
Approval Date
Sep 19, 2024
NMPA

Moxifloxacin Hydrochloride Injection

Product Name
盐酸莫西沙星注射液
Approval Number
国药准字H20193431
Approval Date
Aug 23, 2024
NMPA

Azithromycin Granules

Product Name
奇嘉灵
Approval Number
国药准字H20094072
Approval Date
Aug 2, 2024
NMPA

Levocetirizine Dihydrochloride Oral Solution

Product Name
盐酸左西替利嗪口服溶液
Approval Number
国药准字H20244195
Approval Date
Jun 28, 2024
NMPA
  • Prev
  • 1
  • 2
  • 3
  • 4
  • 5
  • 18
  • Next

Clinical Trials

No trials found

News

No news found

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.