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 D01717 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of D01717, including repackagers and relabelers. The FDA regulates D01717 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. D01717 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 D01717 supplier is an individual or a company that provides D01717 active pharmaceutical ingredient (API) or D01717 finished formulations upon request. The D01717 suppliers may include D01717 API manufacturers, exporters, distributors and traders.
click here to find a list of D01717 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A D01717 written confirmation (D01717 WC) is an official document issued by a regulatory agency to a D01717 manufacturer, verifying that the manufacturing facility of a D01717 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting D01717 APIs or D01717 finished pharmaceutical products to another nation, regulatory agencies frequently require a D01717 WC (written confirmation) as part of the regulatory process.
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