Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
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01 1Farmak A.S. Olomouc CZ
02 1WAVELENGTH ENTERPRISES LTD. Petah Tikva IL
03 1NEULAND LABORATORIES LIMITED Hyderabad IN
04 1KINSY, S.L. Murcia ES
05 1ACTAVIS PHARMA MANUFACTURING PRIVATE LIMITED Alathur IN
06 1AREVIPHARMA GMBH Radebeul DE
07 1Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Am Rhein DE
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01 7Moxonidine
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01 1Czech Republic
02 1France
03 2Germany
04 1India
05 1Ireland
06 1Spain
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01 1Expired
02 5Valid
03 1Withdrawn by Holder
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Certificate Number : CEP 2008-266 - Rev 03
Status : Valid
Issue Date : 2023-09-22
Type : Chemical
Substance Number : 1758
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Certificate Number : CEP 2005-009 - Rev 11
Status : Valid
Issue Date : 2024-10-23
Type : Chemical
Substance Number : 1758
Certificate Number : CEP 2013-175 - Rev 03
Status : Valid
Issue Date : 2024-01-30
Type : Chemical
Substance Number : 1758
Reliable Spanish CDMO Delivering High-Quality APIs and Intermediates with Excellence, Flexibility, and Regulatory Compliance.
Reliable Spanish CDMO Delivering High-Quality APIs and Intermediates with Excellence, Flexibility, and Regulatory Compliance.
Certificate Number : R1-CEP 2014-357 - Rev 00
Status : Valid
Issue Date : 2021-06-10
Type : Chemical
Substance Number : 1758
Certificate Number : R0-CEP 2005-292 - Rev 00
Status : Expired
Issue Date : 2007-06-01
Type : Chemical
Substance Number : 1758
Certificate Number : R1-CEP 2013-122 - Rev 00
Status : Valid
Issue Date : 2020-01-09
Type : Chemical
Substance Number : 1758
Certificate Number : R1-CEP 2003-139 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2009-07-29
Type : Chemical
Substance Number : 1758
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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 Physiotens manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Physiotens, including repackagers and relabelers. The FDA regulates Physiotens manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Physiotens 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 Physiotens manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Physiotens supplier is an individual or a company that provides Physiotens active pharmaceutical ingredient (API) or Physiotens finished formulations upon request. The Physiotens suppliers may include Physiotens API manufacturers, exporters, distributors and traders.
click here to find a list of Physiotens suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Physiotens CEP of the European Pharmacopoeia monograph is often referred to as a Physiotens Certificate of Suitability (COS). The purpose of a Physiotens CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Physiotens EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Physiotens to their clients by showing that a Physiotens CEP has been issued for it. The manufacturer submits a Physiotens CEP (COS) as part of the market authorization procedure, and it takes on the role of a Physiotens CEP holder for the record. Additionally, the data presented in the Physiotens CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Physiotens DMF.
A Physiotens CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Physiotens 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 Physiotens suppliers with CEP (COS) on PharmaCompass.
We have 7 companies offering Physiotens
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