Chirogate is a professional Prostaglandin manufacturer.
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01 1CHIROGATE INTERNATIONAL INC. Taoyuan City TW
02 1EUROAPI HUNGARY Ltd. Budapest HU
03 1CAYMAN CHEMICAL COMPANY, INC. Ann Arbor US
04 1GENTEC, S.A. L´Hospitalet de Llobregat ES
05 1EVERLIGHT CHEMICAL INDUSTRIAL CORPORATION Taipei TW
06 1Industriale Chimica S.R.L. Saronno IT
07 1KYOWA PHARMA CHEMICAL CO., LTD. Takaoka JP
08 1MSN LABORATORIES PRIVATE LIMITED Kardanur Village IN
09 1NEWCHEM S.p.A. Milano IT
10 1YS LIFE SCIENCE Co. Ltd. Hwaseong-si KR
11 1ZHEJIANG AUSUN PHARMACEUTICAL CO., LTD. Taizhou CN
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01 11Latanoprost
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01 1China
02 1France
03 1India
04 2Italy
05 1Japan
06 1South Korea
07 1Spain
08 2Taiwan
09 1U.S.A
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01 11Valid
Certificate Number : CEP 2021-379 - Rev 01
Status : Valid
Issue Date : 2024-08-21
Type : Chemical
Substance Number : 2230
Certificate Number : R0-CEP 2021-352 - Rev 00
Status : Valid
Issue Date : 2022-12-02
Type : Chemical
Substance Number : 2230
Certificate Number : CEP 2022-093 - Rev 01
Status : Valid
Issue Date : 2024-11-25
Type : Chemical
Substance Number : 2230
Gentec Pharmaceutical Group is focused on manufacturing & developing APIs/HPAPIs, Advanced Intermediates & Fine Chemicals.
Gentec Pharmaceutical Group is focused on manufacturing & developing APIs/HPAPIs, Advanced Intermediates & Fine Chemicals.
Certificate Number : R0-CEP 2021-059 - Rev 00
Status : Valid
Issue Date : 2023-07-26
Type : Chemical
Substance Number : 2230
Certificate Number : R0-CEP 2021-002 - Rev 00
Status : Valid
Issue Date : 2023-01-17
Type : Chemical
Substance Number : 2230
Certificate Number : CEP 2022-107 - Rev 01
Status : Valid
Issue Date : 2024-01-29
Type : Chemical
Substance Number : 2230
Certificate Number : CEP 2023-113 - Rev 00
Status : Valid
Issue Date : 2024-06-12
Type : Chemical
Substance Number : 2230
Certificate Number : R0-CEP 2020-368 - Rev 02
Status : Valid
Issue Date : 2023-07-21
Type : Chemical
Substance Number : 2230
Certificate Number : CEP 2021-058 - Rev 01
Status : Valid
Issue Date : 2023-12-19
Type : Chemical
Substance Number : 2230
Certificate Number : CEP 2022-174 - Rev 00
Status : Valid
Issue Date : 2023-10-23
Type : Chemical
Substance Number : 2230
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PharmaCompass offers a list of Latanoprost 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 Latanoprost manufacturer or Latanoprost supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Latanoprost manufacturer or Latanoprost supplier.
PharmaCompass also assists you with knowing the Latanoprost API Price utilized in the formulation of products. Latanoprost API Price is not always fixed or binding as the Latanoprost Price is obtained through a variety of data sources. The Latanoprost Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Arulatan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Arulatan, including repackagers and relabelers. The FDA regulates Arulatan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Arulatan 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 Arulatan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Arulatan supplier is an individual or a company that provides Arulatan active pharmaceutical ingredient (API) or Arulatan finished formulations upon request. The Arulatan suppliers may include Arulatan API manufacturers, exporters, distributors and traders.
click here to find a list of Arulatan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Arulatan CEP of the European Pharmacopoeia monograph is often referred to as a Arulatan Certificate of Suitability (COS). The purpose of a Arulatan CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Arulatan EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Arulatan to their clients by showing that a Arulatan CEP has been issued for it. The manufacturer submits a Arulatan CEP (COS) as part of the market authorization procedure, and it takes on the role of a Arulatan CEP holder for the record. Additionally, the data presented in the Arulatan CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Arulatan DMF.
A Arulatan CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Arulatan 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 Arulatan suppliers with CEP (COS) on PharmaCompass.
We have 11 companies offering Arulatan
Get in contact with the supplier of your choice: