01 2PCAS S.A.
02 1Excella GmbH & Co. K.G.
03 1FAREVA LA VALLEE
04 1FDC LIMITED.
05 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
06 1Syn-Tech Chem. & Pharm. Co. , Ltd.
Registration Number : 306MF10098
Registrant's Address : 21,chemin de la Sauvegarde 21 Ecully Parc - CS 33167 69134 Ecully Cedex France
Initial Date of Registration : 2024-07-17
Latest Date of Registration : 2024-07-17
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Timolol maleate (for manufacturing purposes only)
Registration Number : 219MF10315
Registrant's Address : 21,chemin de la Sauvegarde 21 Ecully Parc - CS 33167 69134 Ecully Cedex France
Initial Date of Registration : 2007-10-24
Latest Date of Registration : 2022-08-10
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PharmaCompass offers a list of Timolol Maleate 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 Timolol Maleate manufacturer or Timolol Maleate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Timolol Maleate manufacturer or Timolol Maleate supplier.
PharmaCompass also assists you with knowing the Timolol Maleate API Price utilized in the formulation of products. Timolol Maleate API Price is not always fixed or binding as the Timolol Maleate Price is obtained through a variety of data sources. The Timolol Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Timoptic-XE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Timoptic-XE, including repackagers and relabelers. The FDA regulates Timoptic-XE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Timoptic-XE 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 Timoptic-XE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Timoptic-XE supplier is an individual or a company that provides Timoptic-XE active pharmaceutical ingredient (API) or Timoptic-XE finished formulations upon request. The Timoptic-XE suppliers may include Timoptic-XE API manufacturers, exporters, distributors and traders.
click here to find a list of Timoptic-XE 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 Timoptic-XE Drug Master File in Japan (Timoptic-XE JDMF) empowers Timoptic-XE 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 Timoptic-XE JDMF during the approval evaluation for pharmaceutical products. At the time of Timoptic-XE 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 Timoptic-XE suppliers with JDMF on PharmaCompass.
We have 6 companies offering Timoptic-XE
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