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Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected. 
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01 Farmak A.S. Olomouc CZ (1)
02 WAVELENGTH ENTERPRISES LTD. Petah Tikva IL (1)
03 NEULAND LABORATORIES LIMITED Hyderabad IN (1)
04 ACTAVIS PHARMA MANUFACTURING PRIVATE LIMITED Alathur IN (1)
05 AREVIPHARMA GMBH Radebeul DE (1)
06 Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Am Rhein DE (1)
07 KINSY, S.L. Murcia ES (1)
01 Moxonidine (7)
01 Czech Republic (1)
02 France (1)
03 Germany (2)
04 India (1)
05 Ireland (1)
06 Spain (1)
01 Expired (1)
02 Valid (5)
03 Withdrawn by Holder (1)
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PharmaCompass offers a list of Moxonidine 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 Moxonidine manufacturer or Moxonidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Moxonidine manufacturer or Moxonidine supplier.
PharmaCompass also assists you with knowing the Moxonidine API Price utilized in the formulation of products. Moxonidine API Price is not always fixed or binding as the Moxonidine Price is obtained through a variety of data sources. The Moxonidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Prestwick3_001016 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick3_001016, including repackagers and relabelers. The FDA regulates Prestwick3_001016 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick3_001016 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 Prestwick3_001016 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prestwick3_001016 supplier is an individual or a company that provides Prestwick3_001016 active pharmaceutical ingredient (API) or Prestwick3_001016 finished formulations upon request. The Prestwick3_001016 suppliers may include Prestwick3_001016 API manufacturers, exporters, distributors and traders.
click here to find a list of Prestwick3_001016 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Prestwick3_001016 CEP of the European Pharmacopoeia monograph is often referred to as a Prestwick3_001016 Certificate of Suitability (COS). The purpose of a Prestwick3_001016 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Prestwick3_001016 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Prestwick3_001016 to their clients by showing that a Prestwick3_001016 CEP has been issued for it. The manufacturer submits a Prestwick3_001016 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Prestwick3_001016 CEP holder for the record. Additionally, the data presented in the Prestwick3_001016 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Prestwick3_001016 DMF.
A Prestwick3_001016 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Prestwick3_001016 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 Prestwick3_001016 suppliers with CEP (COS) on PharmaCompass.
We have 7 companies offering Prestwick3_001016
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