Inke S.A: APIs manufacturing plant.
01 1Inke, S.A. Castellbisbal ES
02 1Vamsi Labs Limited Solapur IN
03 1Farmabios SpA Gropello Cairoli IT
04 1FERMION OY Espoo FI
05 1AARTI PHARMALABS LIMITED Mulund (W), Mumbai IN
06 1NEULAND LABORATORIES LIMITED Hyderabad IN
07 1CIPLA LIMITED Mumbai IN
08 2HOVIONE FARMACIENCIA S.A. Loures PT
09 1Industriale Chimica S.R.L. Saronno IT
10 2MELODY HEALTHCARE PVT. LTD. Boisar IN
11 2MSN LABORATORIES PRIVATE LIMITED Rudraram Village IN
12 1MYLAN LABORATORIES LIMITED Hyderabad IN
13 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 03
Status : Valid
Issue Date : 2024-03-05
Type : Chemical
Substance Number : 1765
Axplora is your partner of choice for complex APIs.
Salmeterol Xinafoate, Micronised
Certificate Number : R0-CEP 2018-168 - Rev 00
Status : Valid
Issue Date : 2020-06-12
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
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Certificate Number : R1-CEP 2008-239 - Rev 04
Status : Valid
Issue Date : 2022-10-14
Type : Chemical
Substance Number : 1765
Neuland Laboratories- A dedicated 100% API provider.
Certificate Number : CEP 2011-277 - Rev 03
Status : Valid
Issue Date : 2023-09-12
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Salmeterol Xinafoate manufacturer or Salmeterol Xinafoate supplier.
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.
click here to find a list of Serevent Inhaler and Disks suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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.
click here to find a list of Serevent Inhaler and Disks suppliers with CEP (COS) on PharmaCompass.
We have 13 companies offering Serevent Inhaler and Disks
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