01 1M/s M/s. Pioneer Agro Industries Sanvin Laboratories Private Limited
01 1LEVOCABASTINE HYDROCHLORIDE EP
01 1WC-0174
01 1India
LEVOCABASTINE HYDROCHLORIDE EP
Date of Issue : 2026-01-19
Valid Till : 2028-12-09
Written Confirmation Number : WC-0174
Address of the Firm : Plot No.8,7,6,20 & 24, MIDC Industrial Area, Post Kulgaon, Badlapur, Dist. Thane...
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PharmaCompass offers a list of Levocabastine 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 Levocabastine manufacturer or Levocabastine supplier for your needs.
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PharmaCompass also assists you with knowing the Levocabastine API Price utilized in the formulation of products. Levocabastine API Price is not always fixed or binding as the Levocabastine Price is obtained through a variety of data sources. The Levocabastine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A livocab manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of livocab, including repackagers and relabelers. The FDA regulates livocab manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. livocab 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 livocab supplier is an individual or a company that provides livocab active pharmaceutical ingredient (API) or livocab finished formulations upon request. The livocab suppliers may include livocab API manufacturers, exporters, distributors and traders.
click here to find a list of livocab suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A livocab written confirmation (livocab WC) is an official document issued by a regulatory agency to a livocab manufacturer, verifying that the manufacturing facility of a livocab active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting livocab APIs or livocab finished pharmaceutical products to another nation, regulatory agencies frequently require a livocab WC (written confirmation) as part of the regulatory process.
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