Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1PHARMACEUTICAL WORKS POLPHARMA S.A. Starogard Gdanski PL
02 1SUPRIYA LIFESCIENCE LTD. Mumbai IN
03 1HIKAL LIMITED Bangalore IN
04 1IPCA Laboratories Limited Mumbai IN
05 1SANECA PHARMACEUTICALS A.S. Hlohovec SK
06 1SINBIOTIK S.A. DE C.V. Tlalnepantla de Baz MX
07 1SOLARA ACTIVE PHARMA SCIENCES LIMITED Chennai IN
08 2SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
09 1ZENTIVA K.S. Praha 10 CZ
01 9Pentoxifylline
02 1Pentoxifylline, Site-II
01 1Czech Republic
02 6India
03 1Mexico
04 1Poland
05 1Slovakia
01 1Expired
02 8Valid
03 1Withdrawn by Holder
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Certificate Number : R1-CEP 2004-246 - Rev 05
Status : Valid
Issue Date : 2023-01-27
Type : Chemical
Substance Number : 851
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Certificate Number : R0-CEP 2018-294 - Rev 00
Status : Valid
Issue Date : 2021-01-12
Type : Chemical
Substance Number : 851
Certificate Number : CEP 2005-131 - Rev 04
Status : Valid
Issue Date : 2023-11-07
Type : Chemical
Substance Number : 851
Certificate Number : R0-CEP 2004-185 - Rev 02
Status : Expired
Issue Date : 2006-02-17
Type : Chemical
Substance Number : 851
Certificate Number : R1-CEP 2014-356 - Rev 00
Status : Valid
Issue Date : 2021-10-07
Type : Chemical
Substance Number : 851
Certificate Number : CEP 2019-273 - Rev 01
Status : Valid
Issue Date : 2024-02-15
Type : Chemical
Substance Number : 851
Certificate Number : R1-CEP 2000-127 - Rev 06
Status : Valid
Issue Date : 2020-06-04
Type : Chemical
Substance Number : 851
Certificate Number : CEP 1998-139 - Rev 06
Status : Valid
Issue Date : 2023-10-02
Type : Chemical
Substance Number : 851
Certificate Number : R0-CEP 2016-159 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2017-01-09
Type : Chemical
Substance Number : 851
Certificate Number : R1-CEP 2008-012 - Rev 04
Status : Valid
Issue Date : 2022-05-06
Type : Chemical
Substance Number : 851
A Pentoxifylline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pentoxifylline, including repackagers and relabelers. The FDA regulates Pentoxifylline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pentoxifylline 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 Pentoxifylline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pentoxifylline supplier is an individual or a company that provides Pentoxifylline active pharmaceutical ingredient (API) or Pentoxifylline finished formulations upon request. The Pentoxifylline suppliers may include Pentoxifylline API manufacturers, exporters, distributors and traders.
click here to find a list of Pentoxifylline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pentoxifylline CEP of the European Pharmacopoeia monograph is often referred to as a Pentoxifylline Certificate of Suitability (COS). The purpose of a Pentoxifylline CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Pentoxifylline EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Pentoxifylline to their clients by showing that a Pentoxifylline CEP has been issued for it. The manufacturer submits a Pentoxifylline CEP (COS) as part of the market authorization procedure, and it takes on the role of a Pentoxifylline CEP holder for the record. Additionally, the data presented in the Pentoxifylline CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Pentoxifylline DMF.
A Pentoxifylline CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Pentoxifylline 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 Pentoxifylline suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering Pentoxifylline
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