Inke S.A: APIs manufacturing plant.
01 1Inke, S.A. Castellbisbal ES
02 1VAMSI LABS LIMITED Solapur IN
03 1FERMION OY Espoo FI
04 1CIPLA LIMITED Mumbai IN
05 2HOVIONE FARMACIENCIA S.A. Loures PT
06 1INDUSTRIALE CHIMICA S.R.L. Saronno IT
07 1MELODY HEALTHCARE PRIVATE LIMITED Mumbai IN
08 1MELODY HEALTHCARE PVT. LTD. Boisar IN
09 2MSN LABORATORIES PRIVATE LIMITED Rudraram Village IN
10 1MYLAN LABORATORIES LIMITED Hyderabad IN
11 1NATCO PHARMA LIMITED Hyderabad IN
Inke S.A: APIs manufacturing plant.
Certificate Number : R1-CEP 2007-127 - Rev 00
Status : Valid
Issue Date : 2014-06-16
Type : Chemical
Substance Number : 1765
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
Salmeterol Xinafoate, Non-micronised And Microni...
Certificate Number : CEP 2006-226 - Rev 04
Status : Valid
Issue Date : 2025-06-24
Type : Chemical
Substance Number : 1765
With Fermion, start the journey of your innovative API.
Salmeterol Xinafoate, Micronised
Certificate Number : CEP 2018-044 - Rev 04
Status : Valid
Issue Date : 2024-02-01
Type : Chemical
Substance Number : 1765
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PharmaCompass offers a list of Salmeterol Xinafoate 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 Salmeterol Xinafoate manufacturer or Salmeterol Xinafoate supplier for your needs.
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PharmaCompass also assists you with knowing the Salmeterol Xinafoate API Price utilized in the formulation of products. Salmeterol Xinafoate API Price is not always fixed or binding as the Salmeterol Xinafoate Price is obtained through a variety of data sources. The Salmeterol Xinafoate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Serevent Inhaler and Disks manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Serevent Inhaler and Disks, including repackagers and relabelers. The FDA regulates Serevent Inhaler and Disks manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Serevent Inhaler and Disks 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 Serevent Inhaler and Disks supplier is an individual or a company that provides Serevent Inhaler and Disks active pharmaceutical ingredient (API) or Serevent Inhaler and Disks finished formulations upon request. The Serevent Inhaler and Disks suppliers may include Serevent Inhaler and Disks API manufacturers, exporters, distributors and traders.
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A Serevent Inhaler and Disks CEP of the European Pharmacopoeia monograph is often referred to as a Serevent Inhaler and Disks Certificate of Suitability (COS). The purpose of a Serevent Inhaler and Disks CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Serevent Inhaler and Disks EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Serevent Inhaler and Disks to their clients by showing that a Serevent Inhaler and Disks CEP has been issued for it. The manufacturer submits a Serevent Inhaler and Disks CEP (COS) as part of the market authorization procedure, and it takes on the role of a Serevent Inhaler and Disks CEP holder for the record. Additionally, the data presented in the Serevent Inhaler and Disks CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Serevent Inhaler and Disks DMF.
A Serevent Inhaler and Disks CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Serevent Inhaler and Disks CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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