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
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.
Certificate Number : R0-CEP 2018-294 - Rev 00
Status : Valid
Issue Date : 2021-01-12
Type : Chemical
Substance Number : 851
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PharmaCompass offers a list of Pentoxifylline 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 Pentoxifylline manufacturer or Pentoxifylline supplier for your needs.
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PharmaCompass also assists you with knowing the Pentoxifylline API Price utilized in the formulation of products. Pentoxifylline API Price is not always fixed or binding as the Pentoxifylline Price is obtained through a variety of data sources. The Pentoxifylline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Pentilin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pentilin, including repackagers and relabelers. The FDA regulates Pentilin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pentilin 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 Pentilin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pentilin supplier is an individual or a company that provides Pentilin active pharmaceutical ingredient (API) or Pentilin finished formulations upon request. The Pentilin suppliers may include Pentilin API manufacturers, exporters, distributors and traders.
click here to find a list of Pentilin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pentilin CEP of the European Pharmacopoeia monograph is often referred to as a Pentilin Certificate of Suitability (COS). The purpose of a Pentilin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Pentilin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Pentilin to their clients by showing that a Pentilin CEP has been issued for it. The manufacturer submits a Pentilin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Pentilin CEP holder for the record. Additionally, the data presented in the Pentilin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Pentilin DMF.
A Pentilin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Pentilin 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 Pentilin suppliers with CEP (COS) on PharmaCompass.
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