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
A Timolol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Timolol, including repackagers and relabelers. The FDA regulates Timolol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Timolol 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 Timolol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Timolol supplier is an individual or a company that provides Timolol active pharmaceutical ingredient (API) or Timolol finished formulations upon request. The Timolol suppliers may include Timolol API manufacturers, exporters, distributors and traders.
click here to find a list of Timolol 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 Timolol Drug Master File in Japan (Timolol JDMF) empowers Timolol 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 Timolol JDMF during the approval evaluation for pharmaceutical products. At the time of Timolol 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 Timolol suppliers with JDMF on PharmaCompass.
We have 6 companies offering Timolol
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