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Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide. 
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01 PHARMACEUTICAL WORKS POLPHARMA S.A. Starogard Gdanski PL (1)
02 SUPRIYA LIFESCIENCE LTD. Mumbai IN (1)
03 ZENTIVA K.S. Praha 10 CZ (1)
04 HIKAL LIMITED Bangalore IN (1)
05 IPCA Laboratories Limited Mumbai IN (1)
06 SANECA PHARMACEUTICALS A.S. Hlohovec SK (1)
07 SINBIOTIK S.A. DE C.V. Tlalnepantla de Baz MX (1)
08 SOLARA ACTIVE PHARMA SCIENCES LIMITED Chennai IN (1)
09 SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN (2)
01 Pentoxifylline (9)
02 Pentoxifylline, Site-II (1)
01 Czech Republic (1)
02 India (6)
03 Mexico (1)
04 Poland (1)
05 Slovakia (1)
01 Expired (1)
02 Valid (8)
03 Withdrawn by Holder (1)
CPhI Japan
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pentoxifylline manufacturer or Pentoxifylline supplier.
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 MolPort-001-823-263 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-823-263, including repackagers and relabelers. The FDA regulates MolPort-001-823-263 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-823-263 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 MolPort-001-823-263 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MolPort-001-823-263 supplier is an individual or a company that provides MolPort-001-823-263 active pharmaceutical ingredient (API) or MolPort-001-823-263 finished formulations upon request. The MolPort-001-823-263 suppliers may include MolPort-001-823-263 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-823-263 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MolPort-001-823-263 CEP of the European Pharmacopoeia monograph is often referred to as a MolPort-001-823-263 Certificate of Suitability (COS). The purpose of a MolPort-001-823-263 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MolPort-001-823-263 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MolPort-001-823-263 to their clients by showing that a MolPort-001-823-263 CEP has been issued for it. The manufacturer submits a MolPort-001-823-263 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MolPort-001-823-263 CEP holder for the record. Additionally, the data presented in the MolPort-001-823-263 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MolPort-001-823-263 DMF.
A MolPort-001-823-263 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MolPort-001-823-263 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 MolPort-001-823-263 suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering MolPort-001-823-263
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