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 Deferiprone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Deferiprone, including repackagers and relabelers. The FDA regulates Deferiprone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Deferiprone 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 Deferiprone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Deferiprone supplier is an individual or a company that provides Deferiprone active pharmaceutical ingredient (API) or Deferiprone finished formulations upon request. The Deferiprone suppliers may include Deferiprone API manufacturers, exporters, distributors and traders.
click here to find a list of Deferiprone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Deferiprone CEP of the European Pharmacopoeia monograph is often referred to as a Deferiprone Certificate of Suitability (COS). The purpose of a Deferiprone CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Deferiprone EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Deferiprone to their clients by showing that a Deferiprone CEP has been issued for it. The manufacturer submits a Deferiprone CEP (COS) as part of the market authorization procedure, and it takes on the role of a Deferiprone CEP holder for the record. Additionally, the data presented in the Deferiprone CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Deferiprone DMF.
A Deferiprone CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Deferiprone 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 Deferiprone suppliers with CEP (COS) on PharmaCompass.
We have 2 companies offering Deferiprone
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
