01 1PCAS Ecully FR
02 2NEULAND LABORATORIES LIMITED Hyderabad IN
03 1BACHEM S.A. Vionnaz CH
04 1CURIA SPAIN S.A.U. Boecillo ES
05 1F.I.S. - FABBRICA ITALIANA SINTETICI S.P.A. Montecchio Maggiore IT
06 2FDC Limited Mumbai IN
07 1HETERO DRUGS LIMITED Hyderabad IN
08 2INDOCO REMEDIES LIMITED Mumbai IN
09 2MICRO LABS LIMITED Bengaluru IN
10 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
Certificate Number : R1-CEP 2012-023 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2020-07-30
Type : Chemical
Substance Number : 2359
Neuland Laboratories- A dedicated 100% API provider.
Certificate Number : R1-CEP 2008-155 - Rev 03
Status : Valid
Issue Date : 2021-09-07
Type : Chemical
Substance Number : 2359
Neuland Laboratories- A dedicated 100% API provider.
Dorzolamide Hydrochloride, Process II
Certificate Number : R1-CEP 2017-089 - Rev 00
Status : Valid
Issue Date : 2022-08-22
Type : Chemical
Substance Number : 2359
70
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 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cosopt, including repackagers and relabelers. The FDA regulates Cosopt manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cosopt 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 Cosopt manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cosopt supplier is an individual or a company that provides Cosopt active pharmaceutical ingredient (API) or Cosopt finished formulations upon request. The Cosopt suppliers may include Cosopt API manufacturers, exporters, distributors and traders.
click here to find a list of Cosopt suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cosopt CEP of the European Pharmacopoeia monograph is often referred to as a Cosopt Certificate of Suitability (COS). The purpose of a Cosopt CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cosopt EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cosopt to their clients by showing that a Cosopt CEP has been issued for it. The manufacturer submits a Cosopt CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cosopt CEP holder for the record. Additionally, the data presented in the Cosopt CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cosopt DMF.
A Cosopt CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cosopt CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Cosopt suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering Cosopt
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