01 1OLON S.P.A. Rodano IT
01 1Maprotiline hydrochloride
01 1Italy
01 1Valid
Certificate Number : CEP 2006-290 - Rev 08
Status : Valid
Issue Date : 2024-08-21
Type : Chemical
Substance Number : 1237
49
PharmaCompass offers a list of MAPROTILINE HYDROCHLORIDE 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 MAPROTILINE HYDROCHLORIDE manufacturer or MAPROTILINE HYDROCHLORIDE supplier for your needs.
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PharmaCompass also assists you with knowing the MAPROTILINE HYDROCHLORIDE API Price utilized in the formulation of products. MAPROTILINE HYDROCHLORIDE API Price is not always fixed or binding as the MAPROTILINE HYDROCHLORIDE Price is obtained through a variety of data sources. The MAPROTILINE HYDROCHLORIDE Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MAPROTILINE HYDROCHLORIDE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MAPROTILINE HYDROCHLORIDE, including repackagers and relabelers. The FDA regulates MAPROTILINE HYDROCHLORIDE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MAPROTILINE HYDROCHLORIDE 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 MAPROTILINE HYDROCHLORIDE supplier is an individual or a company that provides MAPROTILINE HYDROCHLORIDE active pharmaceutical ingredient (API) or MAPROTILINE HYDROCHLORIDE finished formulations upon request. The MAPROTILINE HYDROCHLORIDE suppliers may include MAPROTILINE HYDROCHLORIDE API manufacturers, exporters, distributors and traders.
click here to find a list of MAPROTILINE HYDROCHLORIDE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MAPROTILINE HYDROCHLORIDE CEP of the European Pharmacopoeia monograph is often referred to as a MAPROTILINE HYDROCHLORIDE Certificate of Suitability (COS). The purpose of a MAPROTILINE HYDROCHLORIDE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MAPROTILINE HYDROCHLORIDE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MAPROTILINE HYDROCHLORIDE to their clients by showing that a MAPROTILINE HYDROCHLORIDE CEP has been issued for it. The manufacturer submits a MAPROTILINE HYDROCHLORIDE CEP (COS) as part of the market authorization procedure, and it takes on the role of a MAPROTILINE HYDROCHLORIDE CEP holder for the record. Additionally, the data presented in the MAPROTILINE HYDROCHLORIDE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MAPROTILINE HYDROCHLORIDE DMF.
A MAPROTILINE HYDROCHLORIDE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MAPROTILINE HYDROCHLORIDE 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 MAPROTILINE HYDROCHLORIDE suppliers with CEP (COS) on PharmaCompass.
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