DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1M/s Dr. Reddy's Laboratories
02 1M/s. Dr. Reddy’s Laboratories Limited
03 1M/s MSN Laboratories
04 1M/s Natco Organics Limited
05 1MSN Laboratories Pvt. Ltd.
01 1Lenvatinib Mesylate DMSO Solvate IH
02 3Lenvatinib Mesylate IH
03 1Lenvatinib mesilate DMSO Solvate IH
01 1WC-0039
02 1WC-0067
03 1WC-0349
04 1WC-0349A5-A6
05 1WC-0372
01 5India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-06
Valid Till : 2025-07-07
Written Confirmation Number : WC-0039
Address of the Firm : Unit-I, Plot Nos.137, 138, 145 & 146, Sri Venkateswara Co- Operative Industrial ...
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-17
Valid Till : 2025-07-07
Written Confirmation Number : WC-0067
Address of the Firm : Chemical Technical Operations Unit-VI, APIIC Industrial Estate, Pydibhimavaram V...
Lenvatinib Mesylate DMSO Solvate IH
Date of Issue : 2022-09-02
Valid Till : 2025-05-05
Written Confirmation Number : WC-0349
Address of the Firm : MIs. MSN Laboratories Private Limited, Unit-II, sv. No, 50, Kardanur (Village), ...
Lenvatinib mesilate DMSO Solvate IH
Date of Issue : 2019-10-07
Valid Till : 2022-05-05
Written Confirmation Number : WC-0349A5-A6
Address of the Firm : Unit-||, Sy. No. 50, Kardanur Village, Patti/Post Patancheru Mandal,Sangareddy D...
Date of Issue : 2019-10-07
Valid Till : 2022-06-12
Written Confirmation Number : WC-0372
Address of the Firm : S. No. 73/1A, 74/7B, 78/1B, 79/1, 2B 3 4B 5 6A, 6B, 7, 80/1,2 3,4, 84/1, 2, 3A, ...
A Lenvatinib Mesylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lenvatinib Mesylate, including repackagers and relabelers. The FDA regulates Lenvatinib Mesylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lenvatinib Mesylate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Lenvatinib Mesylate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lenvatinib Mesylate supplier is an individual or a company that provides Lenvatinib Mesylate active pharmaceutical ingredient (API) or Lenvatinib Mesylate finished formulations upon request. The Lenvatinib Mesylate suppliers may include Lenvatinib Mesylate API manufacturers, exporters, distributors and traders.
click here to find a list of Lenvatinib Mesylate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lenvatinib Mesylate written confirmation (Lenvatinib Mesylate WC) is an official document issued by a regulatory agency to a Lenvatinib Mesylate manufacturer, verifying that the manufacturing facility of a Lenvatinib Mesylate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Lenvatinib Mesylate APIs or Lenvatinib Mesylate finished pharmaceutical products to another nation, regulatory agencies frequently require a Lenvatinib Mesylate WC (written confirmation) as part of the regulatory process.
click here to find a list of Lenvatinib Mesylate suppliers with Written Confirmation (WC) on PharmaCompass.
We have 3 companies offering Lenvatinib Mesylate
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