01 1Alembic Pharmaceuticals Limited
02 1Huangshi Shixing Pharmaceutical Co. , Ltd.
01 1ROXITHROMYCIN
02 1Roxithromycin
01 1China
02 1India
Registration Number : 218MF10414
Registrant's Address : Alembic Road, Vadodara 390 003, Gujarat, India
Initial Date of Registration : 2006-04-14
Latest Date of Registration : 2025-04-16
Registration Number : 302MF10125
Registrant's Address : No. 73 East Jinshan Road, Huangjinshan Development Zone, Huangshi, Hubei, China
Initial Date of Registration : 2020-10-08
Latest Date of Registration : 2023-10-04
97
PharmaCompass offers a list of Roxithromycin 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 Roxithromycin manufacturer or Roxithromycin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Roxithromycin manufacturer or Roxithromycin supplier.
A Heng Te manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Heng Te, including repackagers and relabelers. The FDA regulates Heng Te manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Heng Te 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 Heng Te manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Heng Te supplier is an individual or a company that provides Heng Te active pharmaceutical ingredient (API) or Heng Te finished formulations upon request. The Heng Te suppliers may include Heng Te API manufacturers, exporters, distributors and traders.
click here to find a list of Heng Te suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Heng Te Drug Master File in Japan (Heng Te JDMF) empowers Heng Te API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Heng Te JDMF during the approval evaluation for pharmaceutical products. At the time of Heng Te JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Heng Te suppliers with JDMF on PharmaCompass.
We have 2 companies offering Heng Te
Get in contact with the supplier of your choice:
