01 3M/sSun Pharmaceutical Industries Ltd
01 1Cilastatin Sodium Sterile USP/Ph. Eur
02 1Imipenem Ph. Eur. and Cilastatin Sodium Ph. Eur.Sterile Blend Ph. Eur
03 1Imipenem USP and Cilastatin Sodium USP (SterileBlend) USP
01 3WC-0216
01 3India
Imipenem USP and Cilastatin Sodium USP (SterileBlend) USP
Date of Issue : 2025-07-10
Valid Till : 2028-07-04
Written Confirmation Number : WC-0216
Address of the Firm : Industrial Area-03, A. B. Road, Dewas
Cilastatin Sodium Sterile USP/Ph. Eur
Date of Issue : 2025-07-10
Valid Till : 2028-07-04
Written Confirmation Number : WC-0216
Address of the Firm : Industrial Area-03, A. B. Road, Dewas
Imipenem Ph. Eur. and Cilastatin Sodium Ph. Eur.Sterile Blend Ph. Eur
Date of Issue : 2025-07-10
Valid Till : 2028-07-04
Written Confirmation Number : WC-0216
Address of the Firm : Industrial Area-03, A. B. Road, Dewas
63
PharmaCompass offers a list of Cilastatin Sodium 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 Cilastatin Sodium manufacturer or Cilastatin Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cilastatin Sodium manufacturer or Cilastatin Sodium supplier.
PharmaCompass also assists you with knowing the Cilastatin Sodium API Price utilized in the formulation of products. Cilastatin Sodium API Price is not always fixed or binding as the Cilastatin Sodium Price is obtained through a variety of data sources. The Cilastatin Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cilastatin Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cilastatin Sodium, including repackagers and relabelers. The FDA regulates Cilastatin Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cilastatin Sodium 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 Cilastatin Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cilastatin Sodium supplier is an individual or a company that provides Cilastatin Sodium active pharmaceutical ingredient (API) or Cilastatin Sodium finished formulations upon request. The Cilastatin Sodium suppliers may include Cilastatin Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Cilastatin Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cilastatin Sodium written confirmation (Cilastatin Sodium WC) is an official document issued by a regulatory agency to a Cilastatin Sodium manufacturer, verifying that the manufacturing facility of a Cilastatin Sodium active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Cilastatin Sodium APIs or Cilastatin Sodium finished pharmaceutical products to another nation, regulatory agencies frequently require a Cilastatin Sodium WC (written confirmation) as part of the regulatory process.
click here to find a list of Cilastatin Sodium suppliers with Written Confirmation (WC) on PharmaCompass.
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