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 1TYCHE INDUSTRIES LIMITED Hyderabad IN
06 1URQUIMA S.A. Palau-solità i Plegamans ES
07 1VASUDHA PHARMA CHEM LIMITED Hyderabad IN
01 6Rupatadine fumarate
02 1Rupatadine fumarate, Micronised, non-micronised
01 1France
02 5India
03 1Spain
01 7Valid
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
Certificate Number : CEP 2018-161 - Rev 02
Status : Valid
Issue Date : 2024-01-25
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 : 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 : R0-CEP 2018-180 - Rev 02
Status : Valid
Issue Date : 2023-02-02
Type : Chemical
Substance Number : 2888
A Rinialer manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rinialer, including repackagers and relabelers. The FDA regulates Rinialer manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rinialer 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 Rinialer manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rinialer supplier is an individual or a company that provides Rinialer active pharmaceutical ingredient (API) or Rinialer finished formulations upon request. The Rinialer suppliers may include Rinialer API manufacturers, exporters, distributors and traders.
click here to find a list of Rinialer suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Rinialer CEP of the European Pharmacopoeia monograph is often referred to as a Rinialer Certificate of Suitability (COS). The purpose of a Rinialer CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Rinialer EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Rinialer to their clients by showing that a Rinialer CEP has been issued for it. The manufacturer submits a Rinialer CEP (COS) as part of the market authorization procedure, and it takes on the role of a Rinialer CEP holder for the record. Additionally, the data presented in the Rinialer CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Rinialer DMF.
A Rinialer CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Rinialer 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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