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01 1M/s Amoli Organics Pvt Ltd
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01 1Sildenafil Citrate EP/USP
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01 1WC-0077
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01 1India
Date of Issue : 2022-06-09
Valid Till : 2025-12-08
Written Confirmation Number : WC-0077
Address of the Firm : Block No. 422, ECP Canal Road Village - Luna, Tal - Padra, Dist - Vadodara GUjar...
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PharmaCompass offers a list of Citric Acid 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 Citric Acid manufacturer or Citric Acid supplier for your needs.
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PharmaCompass also assists you with knowing the Citric Acid API Price utilized in the formulation of products. Citric Acid API Price is not always fixed or binding as the Citric Acid Price is obtained through a variety of data sources. The Citric Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Uralyt U manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Uralyt U, including repackagers and relabelers. The FDA regulates Uralyt U manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Uralyt U API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Uralyt U supplier is an individual or a company that provides Uralyt U active pharmaceutical ingredient (API) or Uralyt U finished formulations upon request. The Uralyt U suppliers may include Uralyt U API manufacturers, exporters, distributors and traders.
click here to find a list of Uralyt U suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Uralyt U written confirmation (Uralyt U WC) is an official document issued by a regulatory agency to a Uralyt U manufacturer, verifying that the manufacturing facility of a Uralyt U active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Uralyt U APIs or Uralyt U finished pharmaceutical products to another nation, regulatory agencies frequently require a Uralyt U WC (written confirmation) as part of the regulatory process.
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