01 1C-SQUARED PHARMA LIMITED Cork IE
02 1ESTEVE QUIMICA S.A. Barcelona ES
01 2Cyclopentolate hydrochloride
01 1Ireland
02 1Spain
01 2Valid
Certificate Number : R0-CEP 2021-469 - Rev 00
Status : Valid
Issue Date : 2023-06-05
Type : Chemical
Substance Number : 1093
Certificate Number : CEP 2016-078 - Rev 01
Status : Valid
Issue Date : 2025-07-30
Type : Chemical
Substance Number : 1093
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PharmaCompass offers a list of Cyclopentolate 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 Cyclopentolate Hydrochloride manufacturer or Cyclopentolate Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cyclopentolate Hydrochloride manufacturer or Cyclopentolate Hydrochloride supplier.
PharmaCompass also assists you with knowing the Cyclopentolate Hydrochloride API Price utilized in the formulation of products. Cyclopentolate Hydrochloride API Price is not always fixed or binding as the Cyclopentolate Hydrochloride Price is obtained through a variety of data sources. The Cyclopentolate Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zyklolat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zyklolat, including repackagers and relabelers. The FDA regulates Zyklolat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zyklolat 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 Zyklolat supplier is an individual or a company that provides Zyklolat active pharmaceutical ingredient (API) or Zyklolat finished formulations upon request. The Zyklolat suppliers may include Zyklolat API manufacturers, exporters, distributors and traders.
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A Zyklolat CEP of the European Pharmacopoeia monograph is often referred to as a Zyklolat Certificate of Suitability (COS). The purpose of a Zyklolat CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Zyklolat EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Zyklolat to their clients by showing that a Zyklolat CEP has been issued for it. The manufacturer submits a Zyklolat CEP (COS) as part of the market authorization procedure, and it takes on the role of a Zyklolat CEP holder for the record. Additionally, the data presented in the Zyklolat CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Zyklolat DMF.
A Zyklolat CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Zyklolat 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 Zyklolat suppliers with CEP (COS) on PharmaCompass.
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