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PharmaCompass offers a list of Azelastine Hydrochloride 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 Azelastine Hydrochloride manufacturer or Azelastine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Azelastine Hydrochloride manufacturer or Azelastine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Azelastine Hydrochloride API Price utilized in the formulation of products. Azelastine Hydrochloride API Price is not always fixed or binding as the Azelastine Hydrochloride Price is obtained through a variety of data sources. The Azelastine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Azelastine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azelastine, including repackagers and relabelers. The FDA regulates Azelastine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azelastine 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 Azelastine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Azelastine supplier is an individual or a company that provides Azelastine active pharmaceutical ingredient (API) or Azelastine finished formulations upon request. The Azelastine suppliers may include Azelastine API manufacturers, exporters, distributors and traders.
click here to find a list of Azelastine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Azelastine CEP of the European Pharmacopoeia monograph is often referred to as a Azelastine Certificate of Suitability (COS). The purpose of a Azelastine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Azelastine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Azelastine to their clients by showing that a Azelastine CEP has been issued for it. The manufacturer submits a Azelastine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Azelastine CEP holder for the record. Additionally, the data presented in the Azelastine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Azelastine DMF.
A Azelastine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Azelastine 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 Azelastine suppliers with CEP (COS) on PharmaCompass.
We have 6 companies offering Azelastine
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