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PharmaCompass offers a list of Pioglitazone 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 Pioglitazone Hydrochloride manufacturer or Pioglitazone Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pioglitazone Hydrochloride manufacturer or Pioglitazone Hydrochloride supplier.
PharmaCompass also assists you with knowing the Pioglitazone Hydrochloride API Price utilized in the formulation of products. Pioglitazone Hydrochloride API Price is not always fixed or binding as the Pioglitazone Hydrochloride Price is obtained through a variety of data sources. The Pioglitazone Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Actos manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Actos, including repackagers and relabelers. The FDA regulates Actos manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Actos 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 Actos manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Actos supplier is an individual or a company that provides Actos active pharmaceutical ingredient (API) or Actos finished formulations upon request. The Actos suppliers may include Actos API manufacturers, exporters, distributors and traders.
click here to find a list of Actos suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Actos CEP of the European Pharmacopoeia monograph is often referred to as a Actos Certificate of Suitability (COS). The purpose of a Actos CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Actos EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Actos to their clients by showing that a Actos CEP has been issued for it. The manufacturer submits a Actos CEP (COS) as part of the market authorization procedure, and it takes on the role of a Actos CEP holder for the record. Additionally, the data presented in the Actos CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Actos DMF.
A Actos CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Actos 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 Actos suppliers with CEP (COS) on PharmaCompass.
We have 7 companies offering Actos
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