Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1AARTI PHARMALABS LIMITED Mulund (W), Mumbai IN
02 1KATWIJK CHEMIE BV Katwijk ZH NL
01 2Deferiprone
01 1India
02 1Netherlands
01 2Valid
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Certificate Number : CEP 2024-124 - Rev 00
Status : Valid
Issue Date : 2024-10-09
Type : Chemical
Substance Number : 2236
Certificate Number : R0-CEP 2020-354 - Rev 00
Status : Valid
Issue Date : 2022-04-19
Type : Chemical
Substance Number : 2236
A Ferriprox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ferriprox, including repackagers and relabelers. The FDA regulates Ferriprox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ferriprox 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 Ferriprox manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ferriprox supplier is an individual or a company that provides Ferriprox active pharmaceutical ingredient (API) or Ferriprox finished formulations upon request. The Ferriprox suppliers may include Ferriprox API manufacturers, exporters, distributors and traders.
click here to find a list of Ferriprox suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ferriprox CEP of the European Pharmacopoeia monograph is often referred to as a Ferriprox Certificate of Suitability (COS). The purpose of a Ferriprox CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ferriprox EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ferriprox to their clients by showing that a Ferriprox CEP has been issued for it. The manufacturer submits a Ferriprox CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ferriprox CEP holder for the record. Additionally, the data presented in the Ferriprox CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ferriprox DMF.
A Ferriprox CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ferriprox 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 Ferriprox suppliers with CEP (COS) on PharmaCompass.
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