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PharmaCompass offers a list of Hydrochlorothiazide 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 Hydrochlorothiazide manufacturer or Hydrochlorothiazide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrochlorothiazide manufacturer or Hydrochlorothiazide supplier.
PharmaCompass also assists you with knowing the Hydrochlorothiazide API Price utilized in the formulation of products. Hydrochlorothiazide API Price is not always fixed or binding as the Hydrochlorothiazide Price is obtained through a variety of data sources. The Hydrochlorothiazide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Acesistem manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acesistem, including repackagers and relabelers. The FDA regulates Acesistem manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acesistem 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 Acesistem manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Acesistem supplier is an individual or a company that provides Acesistem active pharmaceutical ingredient (API) or Acesistem finished formulations upon request. The Acesistem suppliers may include Acesistem API manufacturers, exporters, distributors and traders.
click here to find a list of Acesistem suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Acesistem CEP of the European Pharmacopoeia monograph is often referred to as a Acesistem Certificate of Suitability (COS). The purpose of a Acesistem CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Acesistem EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Acesistem to their clients by showing that a Acesistem CEP has been issued for it. The manufacturer submits a Acesistem CEP (COS) as part of the market authorization procedure, and it takes on the role of a Acesistem CEP holder for the record. Additionally, the data presented in the Acesistem CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Acesistem DMF.
A Acesistem CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Acesistem 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 Acesistem suppliers with CEP (COS) on PharmaCompass.
We have 16 companies offering Acesistem
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