01 1M/s Jubilant Generics Limited
02 1M/s Jubilant Pharmova Limited
03 1M/s MSN Laboratories Private Limited
01 3ALISKIREN HEMIFUMARATE IH
01 1WC-0021n
02 1WC-0092
03 1WC-0092A
01 3India
Date of Issue : 2021-12-02
Valid Till : 2024-11-04
Written Confirmation Number : WC-0092A
Address of the Firm : Plot No. 18, 56, 57& 58, K.I.A.D.B Industrial Area, Nanjangud - 571 302, Mysore ...
Date of Issue : 2022-09-01
Valid Till : 2024-11-04
Written Confirmation Number : WC-0092
Address of the Firm : Plot No. 18, 56, 57 & 58, K.I.A.D.B. Industrial Area\r\nNanjangud - 571 302, Mys...
Date of Issue : 2022-06-17
Valid Till : 2025-07-14
Written Confirmation Number : WC-0021n
Address of the Firm : Sy. Nos: 317, 320, 321, 322, 323, 604 & 605, Rudraram (Village), Patancheru (Man...
A ALISKIREN HEMIFUMARATE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ALISKIREN HEMIFUMARATE, including repackagers and relabelers. The FDA regulates ALISKIREN HEMIFUMARATE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ALISKIREN HEMIFUMARATE 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 ALISKIREN HEMIFUMARATE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ALISKIREN HEMIFUMARATE supplier is an individual or a company that provides ALISKIREN HEMIFUMARATE active pharmaceutical ingredient (API) or ALISKIREN HEMIFUMARATE finished formulations upon request. The ALISKIREN HEMIFUMARATE suppliers may include ALISKIREN HEMIFUMARATE API manufacturers, exporters, distributors and traders.
click here to find a list of ALISKIREN HEMIFUMARATE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ALISKIREN HEMIFUMARATE written confirmation (ALISKIREN HEMIFUMARATE WC) is an official document issued by a regulatory agency to a ALISKIREN HEMIFUMARATE manufacturer, verifying that the manufacturing facility of a ALISKIREN HEMIFUMARATE active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting ALISKIREN HEMIFUMARATE APIs or ALISKIREN HEMIFUMARATE finished pharmaceutical products to another nation, regulatory agencies frequently require a ALISKIREN HEMIFUMARATE WC (written confirmation) as part of the regulatory process.
click here to find a list of ALISKIREN HEMIFUMARATE suppliers with Written Confirmation (WC) on PharmaCompass.
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