Aspen API. More than just an API™
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01 2Fine Chemicals Corporation (Pty) Ltd. Cape Town ZA
02 1FERMION OY Espoo FI
03 2AARTI PHARMALABS LIMITED Mulund (W), Mumbai IN
04 1EXCELLA GMBH & CO. KG Feucht DE
05 1MYLAN LABORATORIES LIMITED Hyderabad IN
06 1Medigraph Pharmaceuticals Pvt. Ltd. Mumbai IN
07 1Microbiologica Quimica e Farmacêutica Ltda Rio De Janeiro BR
08 1RAKSHIT PHARMACEUTICALS LIMITED Vishakhapatnam IN
09 1RPG Life Sciences Limited Navi Mumbai IN
10 1Resolution Chemicals Ltd. Stevenage GB
11 1Zhejiang Cheng Yi Pharmaceutical Co., Ltd. Wenzhou CN
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01 11Azathioprine
02 1Azathioprine, Process 2
03 1Azathioprine, Process 3
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01 1Brazil
02 1China
03 1Finland
04 1Germany
05 5India
06 2South Africa
07 1U.S.A
08 1United Kingdom
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01 2Expired
02 9Valid
03 2Withdrawn by Holder
Certificate Number : R1-CEP 2017-171 - Rev 00
Status : Valid
Issue Date : 2023-02-13
Type : Chemical
Substance Number : 369
Certificate Number : CEP 2006-317 - Rev 02
Status : Valid
Issue Date : 2024-08-23
Type : Chemical
Substance Number : 369
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 2014-030 - Rev 01
Status : Valid
Issue Date : 2022-10-20
Type : Chemical
Substance Number : 369
Certificate Number : R0-CEP 2006-282 - Rev 01
Status : Expired
Issue Date : 2010-06-24
Type : Chemical
Substance Number : 369
Certificate Number : R1-CEP 2001-362 - Rev 04
Status : Valid
Issue Date : 2022-08-29
Type : Chemical
Substance Number : 369
Certificate Number : CEP 2023-216 - Rev 00
Status : Valid
Issue Date : 2024-08-29
Type : Chemical
Substance Number : 369
Certificate Number : R1-CEP 2005-099 - Rev 00
Status : Valid
Issue Date : 2011-09-21
Type : Chemical
Substance Number : 369
Certificate Number : CEP 2001-341 - Rev 10
Status : Valid
Issue Date : 2024-04-12
Type : Chemical
Substance Number : 369
Certificate Number : R1-CEP 2009-400 - Rev 01
Status : Valid
Issue Date : 2016-12-15
Type : Chemical
Substance Number : 369
Certificate Number : CEP 2006-197 - Rev 02
Status : Valid
Issue Date : 2024-07-11
Type : Chemical
Substance Number : 369
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PharmaCompass offers a list of Azathioprine 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 Azathioprine manufacturer or Azathioprine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Azathioprine manufacturer or Azathioprine supplier.
PharmaCompass also assists you with knowing the Azathioprine API Price utilized in the formulation of products. Azathioprine API Price is not always fixed or binding as the Azathioprine Price is obtained through a variety of data sources. The Azathioprine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Imuran manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Imuran, including repackagers and relabelers. The FDA regulates Imuran manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Imuran 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 Imuran manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Imuran supplier is an individual or a company that provides Imuran active pharmaceutical ingredient (API) or Imuran finished formulations upon request. The Imuran suppliers may include Imuran API manufacturers, exporters, distributors and traders.
click here to find a list of Imuran suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Imuran CEP of the European Pharmacopoeia monograph is often referred to as a Imuran Certificate of Suitability (COS). The purpose of a Imuran CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Imuran EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Imuran to their clients by showing that a Imuran CEP has been issued for it. The manufacturer submits a Imuran CEP (COS) as part of the market authorization procedure, and it takes on the role of a Imuran CEP holder for the record. Additionally, the data presented in the Imuran CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Imuran DMF.
A Imuran CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Imuran 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 Imuran suppliers with CEP (COS) on PharmaCompass.
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