01 1HARMAN FINOCHEM LIMITED Mumbai IN
02 1MAC CHEM PRODUCTS (INDIA) PVT. LTD. Mumbai IN
03 1MSN LABORATORIES PRIVATE LIMITED Rudraram Village IN
04 2PATHEON AUSTRIA GMBH & CO. KG Linz AT
05 1SURAJLOK CHEMICALS PVT. LTD. Mumbai IN
01 1Neostigmine bromide
02 5Neostigmine metilsulfate
01 2Austria
02 4India
01 6Valid
Certificate Number : R0-CEP 2019-122 - Rev 01
Status : Valid
Issue Date : 2021-01-08
Type : Chemical
Substance Number : 626
Certificate Number : CEP 2019-024 - Rev 01
Status : Valid
Issue Date : 2024-04-30
Type : Chemical
Substance Number : 626
Certificate Number : R1-CEP 2016-044 - Rev 00
Status : Valid
Issue Date : 2022-09-09
Type : Chemical
Substance Number : 626
Certificate Number : R1-CEP 2003-253 - Rev 02
Status : Valid
Issue Date : 2016-12-15
Type : Chemical
Substance Number : 626
Certificate Number : R1-CEP 2004-084 - Rev 02
Status : Valid
Issue Date : 2016-12-15
Type : Chemical
Substance Number : 46
Certificate Number : CEP 2023-177 - Rev 00
Status : Valid
Issue Date : 2024-09-18
Type : Chemical
Substance Number : 626
52
PharmaCompass offers a list of Neostigmine Methyl Sulfate 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 Neostigmine Methyl Sulfate manufacturer or Neostigmine Methyl Sulfate supplier for your needs.
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PharmaCompass also assists you with knowing the Neostigmine Methyl Sulfate API Price utilized in the formulation of products. Neostigmine Methyl Sulfate API Price is not always fixed or binding as the Neostigmine Methyl Sulfate Price is obtained through a variety of data sources. The Neostigmine Methyl Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Prozerin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prozerin, including repackagers and relabelers. The FDA regulates Prozerin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prozerin 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 Prozerin supplier is an individual or a company that provides Prozerin active pharmaceutical ingredient (API) or Prozerin finished formulations upon request. The Prozerin suppliers may include Prozerin API manufacturers, exporters, distributors and traders.
click here to find a list of Prozerin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Prozerin CEP of the European Pharmacopoeia monograph is often referred to as a Prozerin Certificate of Suitability (COS). The purpose of a Prozerin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Prozerin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Prozerin to their clients by showing that a Prozerin CEP has been issued for it. The manufacturer submits a Prozerin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Prozerin CEP holder for the record. Additionally, the data presented in the Prozerin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Prozerin DMF.
A Prozerin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Prozerin 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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