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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 FLEMING LABORATORIES LIMITED Nawabpet Village IN (1)
03 IPCA LABORATORIES LIMITED Mumbai IN (1)
04 KREATIVE ORGANICS PRIVATE LIMITED Hyderabad IN (1)
05 MITRYCHEM S.A.S. Mitry-Mory FR (1)
06 TARO PHARMACEUTICAL INDUSTRIES, LTD. Haifa Bay IL (1)
07 TEVA PHARMACEUTICAL INDUSTRIES LTD. Petach Tikva IL (1)
08 ZYDUS LIFESCIENCES LIMITED Vadodara IN (1)
09 Zhejiang Chiral Medicine Chemicals Co., Ltd. Hangzhou CN (1)
01 Etodolac (7)
02 Etodolac, Micronised (1)
03 Etodolac, Micronised, non-micronised (1)
01 China (1)
02 France (1)
03 India (4)
04 Israel (1)
05 Poland (1)
06 U.S.A (1)
01 Expired (1)
02 Valid (8)
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PharmaCompass offers a list of Etodolac 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 Etodolac manufacturer or Etodolac supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etodolac manufacturer or Etodolac supplier.
PharmaCompass also assists you with knowing the Etodolac API Price utilized in the formulation of products. Etodolac API Price is not always fixed or binding as the Etodolac Price is obtained through a variety of data sources. The Etodolac Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MolPort-001-759-084 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-759-084, including repackagers and relabelers. The FDA regulates MolPort-001-759-084 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-759-084 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-001-759-084 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MolPort-001-759-084 supplier is an individual or a company that provides MolPort-001-759-084 active pharmaceutical ingredient (API) or MolPort-001-759-084 finished formulations upon request. The MolPort-001-759-084 suppliers may include MolPort-001-759-084 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-759-084 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MolPort-001-759-084 CEP of the European Pharmacopoeia monograph is often referred to as a MolPort-001-759-084 Certificate of Suitability (COS). The purpose of a MolPort-001-759-084 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MolPort-001-759-084 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MolPort-001-759-084 to their clients by showing that a MolPort-001-759-084 CEP has been issued for it. The manufacturer submits a MolPort-001-759-084 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MolPort-001-759-084 CEP holder for the record. Additionally, the data presented in the MolPort-001-759-084 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MolPort-001-759-084 DMF.
A MolPort-001-759-084 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MolPort-001-759-084 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-001-759-084 suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering MolPort-001-759-084
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