01 1Excella GmbH & Co. K.G.
02 1FORMOSA LABORATORIES, INC.
03 1Shilpa Pharma Lifesciences Limited
01 3Temozolomide
01 1India
02 1Luxembourg
03 1Taiwan
Registration Number : 302MF10046
Registrant's Address : NUERNBERGER STRASSE 12, 90537 FEUCHT, GERMANY
Initial Date of Registration : 2020-04-17
Latest Date of Registration : 2020-12-07
Registration Number : 228MF10143
Registrant's Address : 36 Hoping Street, Louchu, Taoyuan 33842, Taiwan
Initial Date of Registration : 2016-08-03
Latest Date of Registration : 2020-04-27
Registration Number : 228MF10125
Registrant's Address : Shilpa House, #12-6-214/A1, Hyderabad Road, Raichur-584 135, Karnataka, India
Initial Date of Registration : 2016-07-12
Latest Date of Registration : 2023-02-15
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PharmaCompass offers a list of Temozolomide 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 Temozolomide manufacturer or Temozolomide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Temozolomide manufacturer or Temozolomide supplier.
PharmaCompass also assists you with knowing the Temozolomide API Price utilized in the formulation of products. Temozolomide API Price is not always fixed or binding as the Temozolomide Price is obtained through a variety of data sources. The Temozolomide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CCRG 81045 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CCRG 81045, including repackagers and relabelers. The FDA regulates CCRG 81045 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CCRG 81045 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 CCRG 81045 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CCRG 81045 supplier is an individual or a company that provides CCRG 81045 active pharmaceutical ingredient (API) or CCRG 81045 finished formulations upon request. The CCRG 81045 suppliers may include CCRG 81045 API manufacturers, exporters, distributors and traders.
click here to find a list of CCRG 81045 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 CCRG 81045 Drug Master File in Japan (CCRG 81045 JDMF) empowers CCRG 81045 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 CCRG 81045 JDMF during the approval evaluation for pharmaceutical products. At the time of CCRG 81045 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 CCRG 81045 suppliers with JDMF on PharmaCompass.
We have 3 companies offering CCRG 81045
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