With Fermion, start the journey of your innovative API.
01 1FERMION OY Espoo FI
02 1CF PHARMA LTD. Budapest HU
03 2EXCELLA GMBH & CO. KG Feucht DE
04 1HUZHOU ZHANWANG PHARMACEUTICAL CO., LTD. Linghu Town CN
05 1Pfizer Limited Sandwich GB
06 1Zhejiang Hisun Pharmaceutical Co., Ltd. Taizhou City CN
01 6Methotrexate
02 1Methotrexate, Base
01 2China
02 1Finland
03 2Germany
04 1Hungary
05 1U.S.A
01 5Valid
02 2Withdrawn by Holder
With Fermion, start the journey of your innovative API.
With Fermion, start the journey of your innovative API.
Certificate Number : R1-CEP 2001-145 - Rev 04
Status : Valid
Issue Date : 2018-10-26
Type : Chemical
Substance Number : 560
CF Pharma- skilled & highly experienced European API producer based in Hungary.
CF Pharma- skilled & highly experienced European API producer based in Hungary.
Certificate Number : R1-CEP 2008-238 - Rev 02
Status : Valid
Issue Date : 2020-02-07
Type : Chemical
Substance Number : 560
Certificate Number : R1-CEP 2000-024 - Rev 10
Status : Valid
Issue Date : 2020-02-21
Type : Chemical
Substance Number : 560
Certificate Number : R0-CEP 2022-373 - Rev 00
Status : Valid
Issue Date : 2022-12-13
Type : Chemical
Substance Number : 560
Certificate Number : R1-CEP 2006-271 - Rev 01
Status : Valid
Issue Date : 2021-02-24
Type : Chemical
Substance Number : 560
Certificate Number : R1-CEP 1996-103 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2004-11-26
Type : Chemical
Substance Number : 560
Certificate Number : R1-CEP 2007-357 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2016-02-11
Type : Chemical
Substance Number : 560
A Methotrexate Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methotrexate Sodium, including repackagers and relabelers. The FDA regulates Methotrexate Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methotrexate Sodium 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 Methotrexate Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methotrexate Sodium supplier is an individual or a company that provides Methotrexate Sodium active pharmaceutical ingredient (API) or Methotrexate Sodium finished formulations upon request. The Methotrexate Sodium suppliers may include Methotrexate Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Methotrexate Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Methotrexate Sodium CEP of the European Pharmacopoeia monograph is often referred to as a Methotrexate Sodium Certificate of Suitability (COS). The purpose of a Methotrexate Sodium CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Methotrexate Sodium EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Methotrexate Sodium to their clients by showing that a Methotrexate Sodium CEP has been issued for it. The manufacturer submits a Methotrexate Sodium CEP (COS) as part of the market authorization procedure, and it takes on the role of a Methotrexate Sodium CEP holder for the record. Additionally, the data presented in the Methotrexate Sodium CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Methotrexate Sodium DMF.
A Methotrexate Sodium CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Methotrexate Sodium 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 Methotrexate Sodium suppliers with CEP (COS) on PharmaCompass.
We have 6 companies offering Methotrexate Sodium
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