IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
01 1PHARMASYNTHESE Saint Pierre Les Elbeuf FR
02 1BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. Hyderabad IN
03 1CADILA PHARMACEUTICALS LIMITED Ankleshwar IN
04 1FDC Limited Mumbai IN
05 1HETERO LABS LIMITED Hyderabad IN
06 1TYCHE INDUSTRIES LIMITED Hyderabad IN
07 1URQUIMA S.A. Palau-solità i Plegamans ES
08 1VASUDHA PHARMA CHEM LIMITED Hyderabad IN
01 6Rupatadine fumarate
02 1Rupatadine fumarate, Micronised and Non-micronised
03 1Rupatadine fumarate, Micronised, non-micronised
01 1France
02 6India
03 1Spain
01 8Valid
IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
Rupatadine Fumarate, Micronised, Non-micronised
Certificate Number : CEP 2021-095 - Rev 00
Status : Valid
Issue Date : 2024-07-10
Type : Chemical
Substance Number : 2888
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Certificate Number : CEP 2023-016 - Rev 00
Status : Valid
Issue Date : 2024-07-09
Type : Chemical
Substance Number : 2888
Rupatadine Fumarate, Micronised And Non-micronis...
Certificate Number : CEP 2018-161 - Rev 03
Status : Valid
Issue Date : 2025-04-25
Type : Chemical
Substance Number : 2888
Certificate Number : CEP 2024-018 - Rev 00
Status : Valid
Issue Date : 2024-11-06
Type : Chemical
Substance Number : 2888
Certificate Number : CEP 2024-294 - Rev 00
Status : Valid
Issue Date : 2025-09-10
Type : Chemical
Substance Number : 2888
Certificate Number : R0-CEP 2018-213 - Rev 01
Status : Valid
Issue Date : 2022-10-26
Type : Chemical
Substance Number : 2888
Certificate Number : R1-CEP 2017-202 - Rev 00
Status : Valid
Issue Date : 2023-08-09
Type : Chemical
Substance Number : 2888
Certificate Number : CEP 2018-180 - Rev 03
Status : Valid
Issue Date : 2025-04-01
Type : Chemical
Substance Number : 2888
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PharmaCompass offers a list of Rupatadine Fumarate 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 Rupatadine Fumarate manufacturer or Rupatadine Fumarate supplier for your needs.
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PharmaCompass also assists you with knowing the Rupatadine Fumarate API Price utilized in the formulation of products. Rupatadine Fumarate API Price is not always fixed or binding as the Rupatadine Fumarate Price is obtained through a variety of data sources. The Rupatadine Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tamalis manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tamalis, including repackagers and relabelers. The FDA regulates Tamalis manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tamalis 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 Tamalis manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tamalis supplier is an individual or a company that provides Tamalis active pharmaceutical ingredient (API) or Tamalis finished formulations upon request. The Tamalis suppliers may include Tamalis API manufacturers, exporters, distributors and traders.
click here to find a list of Tamalis suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tamalis CEP of the European Pharmacopoeia monograph is often referred to as a Tamalis Certificate of Suitability (COS). The purpose of a Tamalis CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tamalis EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tamalis to their clients by showing that a Tamalis CEP has been issued for it. The manufacturer submits a Tamalis CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tamalis CEP holder for the record. Additionally, the data presented in the Tamalis CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tamalis DMF.
A Tamalis CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tamalis 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 Tamalis suppliers with CEP (COS) on PharmaCompass.
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