01 1M/s Chromo laboratories India Pvt ltd
02 1M/sMSN Laboratories Private Limited
01 1Terbinafine HCL USP/Ph. Eur
02 1Terbinafine IH
01 1WC-0021
02 1WC-0317
01 2India
Date of Issue : 2024-07-18
Valid Till : 2027-06-07
Written Confirmation Number : WC-0317
Address of the Firm : Plot No. 43 & 44, IDA Phase-ll, Pashamylaram, Pashamylaram(V), Patancheru (M), S...
Date of Issue : 2025-07-07
Valid Till : 2028-07-14
Written Confirmation Number : WC-0021
Address of the Firm : Sy. Nos, 317,320,321,322,323,604 & 605, Pincode-502329, Rudraram (Village), Pata...
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PharmaCompass also assists you with knowing the Terbinafine API Price utilized in the formulation of products. Terbinafine API Price is not always fixed or binding as the Terbinafine Price is obtained through a variety of data sources. The Terbinafine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lamisil Tablet manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lamisil Tablet, including repackagers and relabelers. The FDA regulates Lamisil Tablet manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lamisil Tablet 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 Lamisil Tablet supplier is an individual or a company that provides Lamisil Tablet active pharmaceutical ingredient (API) or Lamisil Tablet finished formulations upon request. The Lamisil Tablet suppliers may include Lamisil Tablet API manufacturers, exporters, distributors and traders.
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A Lamisil Tablet written confirmation (Lamisil Tablet WC) is an official document issued by a regulatory agency to a Lamisil Tablet manufacturer, verifying that the manufacturing facility of a Lamisil Tablet active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Lamisil Tablet APIs or Lamisil Tablet finished pharmaceutical products to another nation, regulatory agencies frequently require a Lamisil Tablet WC (written confirmation) as part of the regulatory process.
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