01 1M/s Gland Pharma Limited
01 1Enoxaparin Sodium Ph.Eur
01 1WC-0356
01 1India
Date of Issue : 2020-02-10
Valid Till : 2022-02-02
Written Confirmation Number : WC-0356
Address of the Firm : Block C, Phase-I Visakhapatnam Special Economic Zone, Andhra Pradesh, India
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PharmaCompass offers a list of Enoxaparin 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 Enoxaparin Sodium manufacturer or Enoxaparin Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Enoxaparin Sodium API Price utilized in the formulation of products. Enoxaparin Sodium API Price is not always fixed or binding as the Enoxaparin Sodium Price is obtained through a variety of data sources. The Enoxaparin Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lovenox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lovenox, including repackagers and relabelers. The FDA regulates Lovenox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lovenox 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 Lovenox manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lovenox supplier is an individual or a company that provides Lovenox active pharmaceutical ingredient (API) or Lovenox finished formulations upon request. The Lovenox suppliers may include Lovenox API manufacturers, exporters, distributors and traders.
click here to find a list of Lovenox suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lovenox written confirmation (Lovenox WC) is an official document issued by a regulatory agency to a Lovenox manufacturer, verifying that the manufacturing facility of a Lovenox active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Lovenox APIs or Lovenox finished pharmaceutical products to another nation, regulatory agencies frequently require a Lovenox WC (written confirmation) as part of the regulatory process.
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