01 1M/s. Asence Pharma Pvt Ltd
01 1Hydroxycarbamide BP/EP, Hydroxyurea IP/USP
01 1WC-0597
01 1India
Hydroxycarbamide BP/EP, Hydroxyurea IP/USP
Date of Issue : 2024-11-14
Valid Till : 2027-11-13
Written Confirmation Number : WC-0597
Address of the Firm : Survey No. 543 & 603, Sarabhai Campus, Opp. Ranoli Railway Station, Village Rano...
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PharmaCompass offers a list of Hydroxyurea 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 Hydroxyurea manufacturer or Hydroxyurea supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydroxyurea manufacturer or Hydroxyurea supplier.
PharmaCompass also assists you with knowing the Hydroxyurea API Price utilized in the formulation of products. Hydroxyurea API Price is not always fixed or binding as the Hydroxyurea Price is obtained through a variety of data sources. The Hydroxyurea Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Litalir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Litalir, including repackagers and relabelers. The FDA regulates Litalir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Litalir 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 Litalir supplier is an individual or a company that provides Litalir active pharmaceutical ingredient (API) or Litalir finished formulations upon request. The Litalir suppliers may include Litalir API manufacturers, exporters, distributors and traders.
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A Litalir written confirmation (Litalir WC) is an official document issued by a regulatory agency to a Litalir manufacturer, verifying that the manufacturing facility of a Litalir active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Litalir APIs or Litalir finished pharmaceutical products to another nation, regulatory agencies frequently require a Litalir WC (written confirmation) as part of the regulatory process.
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