01 1AREVIPHARMA GMBH Radebeul DE
02 1EVONIK DEGUSSA GMBH Essen DE
03 1HAS HEALTHCARE ADVANCED SYNTHESIS SA Biasca CH
04 1MAITHRI LABORATORIES PRIVATE LIMITED Gaddapotharam Village IN
05 1PATHEON AUSTRIA GMBH & CO. KG Linz AT
06 1Procos S.P.A. Cameri IT
01 6Pyridostigmine bromide
01 1Austria
02 2Germany
03 1India
04 1Italy
05 1Switzerland
01 1Expired
02 5Valid
Certificate Number : CEP 2008-111 - Rev 03
Status : Valid
Issue Date : 2024-05-06
Type : Chemical
Substance Number : 1255
Certificate Number : R1-CEP 2001-348 - Rev 04
Status : Valid
Issue Date : 2022-03-01
Type : Chemical
Substance Number : 1255
Certificate Number : CEP 2021-085 - Rev 01
Status : Valid
Issue Date : 2024-05-03
Type : Chemical
Substance Number : 1255
Certificate Number : R1-CEP 2003-117 - Rev 03
Status : Valid
Issue Date : 2016-12-15
Type : Chemical
Substance Number : 1255
Certificate Number : CEP 2009-211 - Rev 01
Status : Valid
Issue Date : 2023-11-17
Type : Chemical
Substance Number : 1255
Certificate Number : R0-CEP 2005-139 - Rev 03
Status : Expired
Issue Date : 2007-12-05
Type : Chemical
Substance Number : 1255
89
PharmaCompass offers a list of Pyridostigmine 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 Pyridostigmine manufacturer or Pyridostigmine supplier for your needs.
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PharmaCompass also assists you with knowing the Pyridostigmine API Price utilized in the formulation of products. Pyridostigmine API Price is not always fixed or binding as the Pyridostigmine Price is obtained through a variety of data sources. The Pyridostigmine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lefaxin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lefaxin, including repackagers and relabelers. The FDA regulates Lefaxin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lefaxin 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 Lefaxin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lefaxin supplier is an individual or a company that provides Lefaxin active pharmaceutical ingredient (API) or Lefaxin finished formulations upon request. The Lefaxin suppliers may include Lefaxin API manufacturers, exporters, distributors and traders.
click here to find a list of Lefaxin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lefaxin CEP of the European Pharmacopoeia monograph is often referred to as a Lefaxin Certificate of Suitability (COS). The purpose of a Lefaxin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lefaxin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lefaxin to their clients by showing that a Lefaxin CEP has been issued for it. The manufacturer submits a Lefaxin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lefaxin CEP holder for the record. Additionally, the data presented in the Lefaxin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lefaxin DMF.
A Lefaxin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lefaxin 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 Lefaxin suppliers with CEP (COS) on PharmaCompass.
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