Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
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01 1M/s. Symbiotec Pharmalab Ltd
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01 1Prednisolone BP/EP/USP
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01 1WC-0162A2
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01 1India
Date of Issue : 2022-08-31
Valid Till : 2025-07-02
Written Confirmation Number : WC-0162A2
Address of the Firm : Plot No. 5, 6, 7 & 8 Special Economic Zone, Phase II, Pithampur, Dist: Dhar, MP-...
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PharmaCompass offers a list of Prednisolone 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 Prednisolone manufacturer or Prednisolone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Prednisolone manufacturer or Prednisolone supplier.
PharmaCompass also assists you with knowing the Prednisolone API Price utilized in the formulation of products. Prednisolone API Price is not always fixed or binding as the Prednisolone Price is obtained through a variety of data sources. The Prednisolone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Di Adreson F manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Di Adreson F, including repackagers and relabelers. The FDA regulates Di Adreson F manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Di Adreson F 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 Di Adreson F supplier is an individual or a company that provides Di Adreson F active pharmaceutical ingredient (API) or Di Adreson F finished formulations upon request. The Di Adreson F suppliers may include Di Adreson F API manufacturers, exporters, distributors and traders.
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A Di Adreson F written confirmation (Di Adreson F WC) is an official document issued by a regulatory agency to a Di Adreson F manufacturer, verifying that the manufacturing facility of a Di Adreson F active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Di Adreson F APIs or Di Adreson F finished pharmaceutical products to another nation, regulatory agencies frequently require a Di Adreson F WC (written confirmation) as part of the regulatory process.
click here to find a list of Di Adreson F suppliers with Written Confirmation (WC) on PharmaCompass.
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