01 1M/s Abhilasha Pharma Pvt Ltd
01 1Pioglitazone IP/USP
01 1WC-0325
01 1India
Date of Issue : 2022-11-18
Valid Till : 2025-02-18
Written Confirmation Number : WC-0325
Address of the Firm : M/s. Abhilasha Pharma Pvt. Ltd, Plot No. 1408/1409, G.I.D.C, Near Buch Plastic U...
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PharmaCompass offers a list of Pioglitazone 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 manufacturer or Pioglitazone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pioglitazone manufacturer or Pioglitazone supplier.
PharmaCompass also assists you with knowing the Pioglitazone API Price utilized in the formulation of products. Pioglitazone API Price is not always fixed or binding as the Pioglitazone Price is obtained through a variety of data sources. The Pioglitazone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Duetact manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Duetact, including repackagers and relabelers. The FDA regulates Duetact manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Duetact 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 Duetact manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Duetact supplier is an individual or a company that provides Duetact active pharmaceutical ingredient (API) or Duetact finished formulations upon request. The Duetact suppliers may include Duetact API manufacturers, exporters, distributors and traders.
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A Duetact written confirmation (Duetact WC) is an official document issued by a regulatory agency to a Duetact manufacturer, verifying that the manufacturing facility of a Duetact active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Duetact APIs or Duetact finished pharmaceutical products to another nation, regulatory agencies frequently require a Duetact WC (written confirmation) as part of the regulatory process.
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