01 1AURORE LIFE SCIENCES PRIVATE LIMITED Hyderabad IN
02 2HETERO DRUGS LIMITED Hyderabad IN
03 1MAITHRI LABORATORIES PRIVATE LIMITED Gaddapotharam Village IN
04 1OLON S.P.A. Rodano IT
05 1SHANGHAI PHARMA GROUP CHANGZHOU KONY PHARMACEUTICAL CO., LTD. Luoyang Town CN
06 1ZHEJIANG CHARIOTEER PHARMACEUTICAL CO., LTD Xianju CN
01 4Valganciclovir hydrochloride
02 1Valganciclovir hydrochloride, Crystalline Type II
03 1Valganciclovir hydrochloride, Crystalline form
04 1Valganciclovir hydrochloride, Site-II
01 2China
02 4India
03 1Italy
01 7Valid
Certificate Number : CEP 2023-375 - Rev 00
Status : Valid
Issue Date : 2024-12-17
Type : Chemical
Substance Number : 2930
Certificate Number : CEP 2023-414 - Rev 00
Status : Valid
Issue Date : 2025-05-02
Type : Chemical
Substance Number : 2930
Valganciclovir Hydrochloride, Site-II
Certificate Number : CEP 2024-111 - Rev 00
Status : Valid
Issue Date : 2024-04-24
Type : Chemical
Substance Number : 2930
Certificate Number : CEP 2022-398 - Rev 01
Status : Valid
Issue Date : 2025-02-26
Type : Chemical
Substance Number : 2930
Valganciclovir Hydrochloride, Crystalline Form
Certificate Number : CEP 2023-285 - Rev 00
Status : Valid
Issue Date : 2025-07-28
Type : Chemical
Substance Number : 2930
Valganciclovir Hydrochloride, Crystalline Type I...
Certificate Number : CEP 2023-217 - Rev 00
Status : Valid
Issue Date : 2025-04-29
Type : Chemical
Substance Number : 2930
Certificate Number : CEP 2024-326 - Rev 00
Status : Valid
Issue Date : 2025-11-21
Type : Chemical
Substance Number : 2930
71
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A CAS-175865-59-5 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-175865-59-5, including repackagers and relabelers. The FDA regulates CAS-175865-59-5 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-175865-59-5 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 CAS-175865-59-5 supplier is an individual or a company that provides CAS-175865-59-5 active pharmaceutical ingredient (API) or CAS-175865-59-5 finished formulations upon request. The CAS-175865-59-5 suppliers may include CAS-175865-59-5 API manufacturers, exporters, distributors and traders.
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A CAS-175865-59-5 CEP of the European Pharmacopoeia monograph is often referred to as a CAS-175865-59-5 Certificate of Suitability (COS). The purpose of a CAS-175865-59-5 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CAS-175865-59-5 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CAS-175865-59-5 to their clients by showing that a CAS-175865-59-5 CEP has been issued for it. The manufacturer submits a CAS-175865-59-5 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CAS-175865-59-5 CEP holder for the record. Additionally, the data presented in the CAS-175865-59-5 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CAS-175865-59-5 DMF.
A CAS-175865-59-5 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CAS-175865-59-5 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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We have 6 companies offering CAS-175865-59-5
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