Axplora- The partner of choice for complex APIs.
01 1PharmaZell GmbH Raubling DE
02 1Moehs Iberica S.L. Rubi ES
03 1AREVIPHARMA GMBH Radebeul DE
04 1BACHEM S.A. Vionnaz CH
05 1F.I.S. - FABBRICA ITALIANA SINTETICI S.P.A. Montecchio Maggiore IT
06 1Nippon Protein Co., Ltd. Ashikaga-shi JP
07 1Nippon Rika Co., Ltd. Tokyo JP
08 1Protchem Industries (India) Ltd Chennai IN
09 1SEVEN STAR PHARMACEUTICAL COMPANY, LTD. New Taipei City TW
10 2WUHAN GRAND HOYO CO., LTD. Wuhan CN
Axplora- The partner of choice for complex APIs.
Certificate Number : R2-CEP 1995-028 - Rev 04
Status : Valid
Issue Date : 2020-12-15
Type : Chemical
Substance Number : 967
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Certificate Number : R1-CEP 1996-002 - Rev 06
Status : Valid
Issue Date : 2021-04-16
Type : Chemical
Substance Number : 967
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PharmaCompass offers a list of Acetylcysteine 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 Acetylcysteine manufacturer or Acetylcysteine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Acetylcysteine manufacturer or Acetylcysteine supplier.
PharmaCompass also assists you with knowing the Acetylcysteine API Price utilized in the formulation of products. Acetylcysteine API Price is not always fixed or binding as the Acetylcysteine Price is obtained through a variety of data sources. The Acetylcysteine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Acetylcysteine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acetylcysteine, including repackagers and relabelers. The FDA regulates Acetylcysteine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acetylcysteine 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 Acetylcysteine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Acetylcysteine supplier is an individual or a company that provides Acetylcysteine active pharmaceutical ingredient (API) or Acetylcysteine finished formulations upon request. The Acetylcysteine suppliers may include Acetylcysteine API manufacturers, exporters, distributors and traders.
click here to find a list of Acetylcysteine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Acetylcysteine CEP of the European Pharmacopoeia monograph is often referred to as a Acetylcysteine Certificate of Suitability (COS). The purpose of a Acetylcysteine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Acetylcysteine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Acetylcysteine to their clients by showing that a Acetylcysteine CEP has been issued for it. The manufacturer submits a Acetylcysteine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Acetylcysteine CEP holder for the record. Additionally, the data presented in the Acetylcysteine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Acetylcysteine DMF.
A Acetylcysteine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Acetylcysteine 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 Acetylcysteine suppliers with CEP (COS) on PharmaCompass.
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