01 1Curia Spain S. A. U.
02 1F. I. S. Fabrica Italiana Sintetici S. p. A.
03 1FDC LIMITED.
04 2MICRO LABS LIMITED.
01 4Dorzolamide Hydrochloride
02 1Dorzolamide hydrochloride
01 3India
02 1Italy
03 1U.S.A
Registration Number : 227MF10011
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2015-01-05
Latest Date of Registration : 2017-11-21
Registration Number : 230MF10165
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2018-12-04
Latest Date of Registration : 2018-12-04
Registration Number : 306MF10124
Registrant's Address : 142-48,s,v,road,jogeshwari(w),mumbai-400 102 India
Initial Date of Registration : 2024-09-11
Latest Date of Registration : 2024-09-11
Registration Number : 229MF10037
Registrant's Address : 27, RACE COURSE ROAD, BANGALORE-560001, INDIA
Initial Date of Registration : 2017-02-08
Latest Date of Registration : 2017-02-08
Registration Number : 304MF10044
Registrant's Address : 31, Race Course Road, Bengaluru-560 001, KARNATAKA, INDIA
Initial Date of Registration : 2022-02-24
Latest Date of Registration : 2022-02-24
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PharmaCompass offers a list of Dorzolamide Hydrochloride 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 Dorzolamide Hydrochloride manufacturer or Dorzolamide Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dorzolamide Hydrochloride manufacturer or Dorzolamide Hydrochloride supplier.
PharmaCompass also assists you with knowing the Dorzolamide Hydrochloride API Price utilized in the formulation of products. Dorzolamide Hydrochloride API Price is not always fixed or binding as the Dorzolamide Hydrochloride Price is obtained through a variety of data sources. The Dorzolamide Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A COSOPT PF manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of COSOPT PF, including repackagers and relabelers. The FDA regulates COSOPT PF manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. COSOPT PF API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A COSOPT PF supplier is an individual or a company that provides COSOPT PF active pharmaceutical ingredient (API) or COSOPT PF finished formulations upon request. The COSOPT PF suppliers may include COSOPT PF API manufacturers, exporters, distributors and traders.
click here to find a list of COSOPT PF 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 COSOPT PF Drug Master File in Japan (COSOPT PF JDMF) empowers COSOPT PF 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 COSOPT PF JDMF during the approval evaluation for pharmaceutical products. At the time of COSOPT PF JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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