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