01 1CAMBREX CHARLES CITY, INC. Charles City US
02 1CHR. OLESEN SYNTHESIS A/S Hvidovre DK
03 1SPECGX LLC Webster Groves US
01 3Dexamfetamine sulfate
01 1Denmark
02 2U.S.A
01 3Valid
Certificate Number : R0-CEP 2021-478 - Rev 00
Status : Valid
Issue Date : 2023-06-15
Type : Chemical
Substance Number : 2752
Certificate Number : CEP 2019-097 - Rev 01
Status : Valid
Issue Date : 2025-01-03
Type : Chemical
Substance Number : 2752
Certificate Number : R0-CEP 2020-076 - Rev 00
Status : Valid
Issue Date : 2021-07-26
Type : Chemical
Substance Number : 2752
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PharmaCompass offers a list of Amphetamine 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 Amphetamine manufacturer or Amphetamine supplier for your needs.
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PharmaCompass also assists you with knowing the Amphetamine API Price utilized in the formulation of products. Amphetamine API Price is not always fixed or binding as the Amphetamine Price is obtained through a variety of data sources. The Amphetamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 2C9H13N.H2O4S manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2C9H13N.H2O4S, including repackagers and relabelers. The FDA regulates 2C9H13N.H2O4S manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2C9H13N.H2O4S 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 2C9H13N.H2O4S supplier is an individual or a company that provides 2C9H13N.H2O4S active pharmaceutical ingredient (API) or 2C9H13N.H2O4S finished formulations upon request. The 2C9H13N.H2O4S suppliers may include 2C9H13N.H2O4S API manufacturers, exporters, distributors and traders.
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A 2C9H13N.H2O4S CEP of the European Pharmacopoeia monograph is often referred to as a 2C9H13N.H2O4S Certificate of Suitability (COS). The purpose of a 2C9H13N.H2O4S CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 2C9H13N.H2O4S EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 2C9H13N.H2O4S to their clients by showing that a 2C9H13N.H2O4S CEP has been issued for it. The manufacturer submits a 2C9H13N.H2O4S CEP (COS) as part of the market authorization procedure, and it takes on the role of a 2C9H13N.H2O4S CEP holder for the record. Additionally, the data presented in the 2C9H13N.H2O4S CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 2C9H13N.H2O4S DMF.
A 2C9H13N.H2O4S CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 2C9H13N.H2O4S 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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We have 3 companies offering 2C9H13N.H2O4S
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