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01 1M/s Tianish Laboratories Privte Lmited
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01 1Telbivudine IH
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01 1WC-0117
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01 1India
Date of Issue : 2022-06-22
Valid Till : 2025-07-28
Written Confirmation Number : WC-0117
Address of the Firm : Plot No. 14, 99, 100, IDA, Pashmylaram, Phase ? II, Patancheru, Sangareddy Distr...
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PharmaCompass offers a list of Telbivudine 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 Telbivudine manufacturer or Telbivudine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Telbivudine manufacturer or Telbivudine supplier.
PharmaCompass also assists you with knowing the Telbivudine API Price utilized in the formulation of products. Telbivudine API Price is not always fixed or binding as the Telbivudine Price is obtained through a variety of data sources. The Telbivudine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LLT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LLT, including repackagers and relabelers. The FDA regulates LLT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LLT API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A LLT supplier is an individual or a company that provides LLT active pharmaceutical ingredient (API) or LLT finished formulations upon request. The LLT suppliers may include LLT API manufacturers, exporters, distributors and traders.
click here to find a list of LLT suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A LLT written confirmation (LLT WC) is an official document issued by a regulatory agency to a LLT manufacturer, verifying that the manufacturing facility of a LLT active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting LLT APIs or LLT finished pharmaceutical products to another nation, regulatory agencies frequently require a LLT WC (written confirmation) as part of the regulatory process.
click here to find a list of LLT suppliers with Written Confirmation (WC) on PharmaCompass.
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