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Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions. 
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01 NOVACYL Ecully FR (1)
02 Alta Laboratories Ltd Khopoli IN (1)
03 Bayer Hispania, S.L. La Felguera ES (1)
04 Chimprod SA Oradea RO (1)
05 Industria Quimica Andina & Cia. S.A. Bogota D.C CO (1)
06 Jilin Pharmaceutical Co Ltd Jilin City CN (1)
07 SHANDONG XINHUA PHARMACEUTICAL CO., LTD. Zibo CN (1)
08 The Andhra Sugars Limited Tanuku IN (1)
09 WP MANNHEIM GMBH Mannheim DE (1)
01 Acetylsalicylic acid (7)
02 Acetylsalicylic acid, Crystals 7010/7011, fines 7012, granules 7017/7018, granular powder 7028, PR powder 7029 (1)
03 Acetylsalicylic acid, Type 100/300, Type 100/500, Type 300/500, Type 300/800, Type 500/800 (1)
01 China (1)
02 France (1)
03 Germany (2)
04 India (3)
05 Romania (1)
06 U.S.A (1)
01 Expired (1)
02 Valid (4)
03 Withdrawn by EDQM Failure to CEP procedure (3)
04 Withdrawn by Holder (1)
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PharmaCompass offers a list of Aspirin 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 Aspirin manufacturer or Aspirin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aspirin manufacturer or Aspirin supplier.
PharmaCompass also assists you with knowing the Aspirin API Price utilized in the formulation of products. Aspirin API Price is not always fixed or binding as the Aspirin Price is obtained through a variety of data sources. The Aspirin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Asasantin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Asasantin, including repackagers and relabelers. The FDA regulates Asasantin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Asasantin 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 Asasantin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Asasantin supplier is an individual or a company that provides Asasantin active pharmaceutical ingredient (API) or Asasantin finished formulations upon request. The Asasantin suppliers may include Asasantin API manufacturers, exporters, distributors and traders.
click here to find a list of Asasantin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Asasantin CEP of the European Pharmacopoeia monograph is often referred to as a Asasantin Certificate of Suitability (COS). The purpose of a Asasantin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Asasantin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Asasantin to their clients by showing that a Asasantin CEP has been issued for it. The manufacturer submits a Asasantin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Asasantin CEP holder for the record. Additionally, the data presented in the Asasantin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Asasantin DMF.
A Asasantin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Asasantin 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 Asasantin suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering Asasantin
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