Qingmu Pharma: Patients first, FDA/CEP/US-DMF/US-VMF/ASMF APIs for Humans & Vets in 100+ countries.

Reset all filters
01 1Sichuan Qingmu Pharmaceutical
02 1Biophore India Pharmaceuticals Pvt Ltd
03 1Dr. Reddy's Laboratories
04 1Egis Pharmaceuticals PLC
05 1Granules India Limited
06 1Asymchem Laboratories
07 1Beijing Sjar Technology Development
08 1Daishang Pharmchem Group
09 1MSN Laboratories
10 1Macleods Pharmaceuticals Limited
Reset all filters
01 4China
02 1Hungary
03 5India
Reset all filters
01 2Active
02 8Blank
01 10Blank
Reset all filters
01 10Blank
Reset all filters
01 10Blank
Reset all filters
01 1Su108-12-ND
02 9Blank
Reset all filters
01 154893-0524
02 172015-004
03 8Blank
01 10Blank
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 43866
Submission : 2026-03-30
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 43852
Submission : 2026-03-30
Status : Active
Type : II
NDC Package Code : 54893-0524
Start Marketing Date : 2026-03-30
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

NDC Package Code : 72015-004
Start Marketing Date : 2023-11-08
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Takeda Pharmaceutical Korea
Registration Date : 2025-03-06
Registration Number : Su108-12-ND
Manufacturer Name : Tianjin Asymchem Pharmaceuticals Co., Ltd.
Manufacturer Address : No. 71, Xinye 7th Avenue, TEDA WEST Tianjin, 300462, PR




52
PharmaCompass offers a list of Fruquintinib API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Fruquintinib manufacturer or Fruquintinib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fruquintinib manufacturer or Fruquintinib supplier.
A Fruquintinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fruquintinib, including repackagers and relabelers. The FDA regulates Fruquintinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fruquintinib API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Fruquintinib manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Fruquintinib supplier is an individual or a company that provides Fruquintinib active pharmaceutical ingredient (API) or Fruquintinib finished formulations upon request. The Fruquintinib suppliers may include Fruquintinib API manufacturers, exporters, distributors and traders.
click here to find a list of Fruquintinib suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
We have 10 companies offering Fruquintinib
Get in contact with the supplier of your choice: