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 1SOLARA ACTIVE PHARMA SCIENCES LIMITED Chennai IN
01 2Mesna
01 2India
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 : R1-CEP 2009-127 - Rev 01
Status : Valid
Issue Date : 2022-11-30
Type : Chemical
Substance Number : 1674
Certificate Number : CEP 2015-299 - Rev 01
Status : Valid
Issue Date : 2024-08-20
Type : Chemical
Substance Number : 1674
A Mesna manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mesna, including repackagers and relabelers. The FDA regulates Mesna manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mesna 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 Mesna manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mesna supplier is an individual or a company that provides Mesna active pharmaceutical ingredient (API) or Mesna finished formulations upon request. The Mesna suppliers may include Mesna API manufacturers, exporters, distributors and traders.
click here to find a list of Mesna suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Mesna CEP of the European Pharmacopoeia monograph is often referred to as a Mesna Certificate of Suitability (COS). The purpose of a Mesna CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Mesna EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Mesna to their clients by showing that a Mesna CEP has been issued for it. The manufacturer submits a Mesna CEP (COS) as part of the market authorization procedure, and it takes on the role of a Mesna CEP holder for the record. Additionally, the data presented in the Mesna CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Mesna DMF.
A Mesna CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Mesna 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 Mesna suppliers with CEP (COS) on PharmaCompass.
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