01 1Aurobindo Pharma Limited
02 1Corden Pharma Colorado, Inc.
03 1Langfang Hetian Pharmaceutical Co. , Ltd.
04 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S. P. A.
01 1Ethyl-3,5,6-tri-O-benzyl-D-glucofuranoside
02 2Japan Pharmaceutical Codex tribenoside (production only)
03 1TRIBENOSIDE
01 1China
02 1Germany
03 1India
04 1Italy
Ethyl-3,5,6-tri-O-benzyl-D-glucofuranoside
Registration Number : 227MF10068
Registrant's Address : Plot No. 2, Maitrivihar, Ameerpet, Hyderabad Andhra Pradesh, India
Initial Date of Registration : 2015-03-12
Latest Date of Registration : 2015-03-12
Registration Number : 225MF10037
Registrant's Address : 2075 North 55th Street Boulder, Colorado 80301-2880, U.S. S. A
Initial Date of Registration : 2013-02-20
Latest Date of Registration : 2013-02-20
Registration Number : 225MF10117
Registrant's Address : Xinqiao farm, Wen-an county, Langfang city, Hebei, P. R. China
Initial Date of Registration : 2013-06-11
Latest Date of Registration : 2022-03-24
Registration Number : 227MF10227
Registrant's Address : VIA M. Civitali, 1-20148 MILANO, ITALY
Initial Date of Registration : 2015-09-03
Latest Date of Registration : 2015-09-03
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PharmaCompass offers a list of Tribenoside API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Tribenoside manufacturer or Tribenoside supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tribenoside manufacturer or Tribenoside supplier.
PharmaCompass also assists you with knowing the Tribenoside API Price utilized in the formulation of products. Tribenoside API Price is not always fixed or binding as the Tribenoside Price is obtained through a variety of data sources. The Tribenoside Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glyvenol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glyvenol, including repackagers and relabelers. The FDA regulates Glyvenol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glyvenol 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 Glyvenol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glyvenol supplier is an individual or a company that provides Glyvenol active pharmaceutical ingredient (API) or Glyvenol finished formulations upon request. The Glyvenol suppliers may include Glyvenol API manufacturers, exporters, distributors and traders.
click here to find a list of Glyvenol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Glyvenol Drug Master File in Japan (Glyvenol JDMF) empowers Glyvenol 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 Glyvenol JDMF during the approval evaluation for pharmaceutical products. At the time of Glyvenol 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 Glyvenol suppliers with JDMF on PharmaCompass.
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