Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1M/s Aarti Pharmalabs limited
02 1M/s Aarti Pharmalabs ltd
03 1M/s Glenmark Life Sciences Limited
04 1M/s Glenmark life Sciences limited
05 1M/s Hetero Drugs Limited
06 1M/s Melody healthcare Pvt Ltd
07 1M/s Piramal Pharma Limited
08 1M/s Tianish Laboratories Privte Lmited
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Perindopril Erbumine BP/Ph. Eur
Date of Issue : 2024-05-20
Valid Till : 2027-05-19
Written Confirmation Number : WC-0295
Address of the Firm : D-53, PHASE II, KALYAN SHILL ROAD, DOMBIVLI (E.), DOMBIVLI - 421204, Taluka: Dom...
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Perindopril Erbumine BP/Ph. Eur
Date of Issue : 2022-08-24
Valid Till : 2025-07-29
Written Confirmation Number : WC-0099
Address of the Firm : Plot No.E-50, 50/1 and 59/1, Unit ?IV, MIDC, Tarapur?401506, Taluka: Palghar, Di...
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PharmaCompass offers a list of Perindopril Erbumine 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 Perindopril Erbumine manufacturer or Perindopril Erbumine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Perindopril Erbumine manufacturer or Perindopril Erbumine supplier.
PharmaCompass also assists you with knowing the Perindopril Erbumine API Price utilized in the formulation of products. Perindopril Erbumine API Price is not always fixed or binding as the Perindopril Erbumine Price is obtained through a variety of data sources. The Perindopril Erbumine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Covapril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Covapril, including repackagers and relabelers. The FDA regulates Covapril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Covapril 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 Covapril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Covapril supplier is an individual or a company that provides Covapril active pharmaceutical ingredient (API) or Covapril finished formulations upon request. The Covapril suppliers may include Covapril API manufacturers, exporters, distributors and traders.
click here to find a list of Covapril suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Covapril written confirmation (Covapril WC) is an official document issued by a regulatory agency to a Covapril manufacturer, verifying that the manufacturing facility of a Covapril active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Covapril APIs or Covapril finished pharmaceutical products to another nation, regulatory agencies frequently require a Covapril WC (written confirmation) as part of the regulatory process.
click here to find a list of Covapril suppliers with Written Confirmation (WC) on PharmaCompass.
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