LEBSA- Your strategic API source for niche molecules.
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01 2Laboratorios Espinos Y Bofill S.A. (LEBSA) Cornellà ES
02 1ARCHIMICA S.P.A Lodi IT
03 1EXCELLA GMBH & CO. KG Feucht DE
04 1N.V. ORGANON Oss NL
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01 4Mianserin hydrochloride
02 1Mianserin hydrochloride, Process II
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01 1Germany
02 1Italy
03 2Spain
04 1U.S.A
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01 1Expired
02 3Valid
03 1Withdrawn by Holder
Mianserin Hydrochloride, Process II
Certificate Number : R0-CEP 2021-183 - Rev 01
Status : Valid
Issue Date : 2022-05-20
Type : Chemical
Substance Number : 846
Certificate Number : CEP 2022-250 - Rev 00
Status : Valid
Issue Date : 2024-11-28
Type : Chemical
Substance Number : 846
Certificate Number : CEP 2002-055 - Rev 07
Status : Valid
Issue Date : 2024-06-06
Type : Chemical
Substance Number : 846
Certificate Number : R1-CEP 1996-095 - Rev 05
Status : Withdrawn by Holder
Issue Date : 2009-06-16
Type : Chemical
Substance Number : 846
Certificate Number : R0-CEP 2015-335 - Rev 00
Status : Expired
Issue Date : 2017-01-27
Type : Chemical
Substance Number : 846
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PharmaCompass offers a list of Mianserin 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 Mianserin Hydrochloride manufacturer or Mianserin Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mianserin Hydrochloride manufacturer or Mianserin Hydrochloride supplier.
PharmaCompass also assists you with knowing the Mianserin Hydrochloride API Price utilized in the formulation of products. Mianserin Hydrochloride API Price is not always fixed or binding as the Mianserin Hydrochloride Price is obtained through a variety of data sources. The Mianserin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tolvon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tolvon, including repackagers and relabelers. The FDA regulates Tolvon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tolvon 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 Tolvon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tolvon supplier is an individual or a company that provides Tolvon active pharmaceutical ingredient (API) or Tolvon finished formulations upon request. The Tolvon suppliers may include Tolvon API manufacturers, exporters, distributors and traders.
click here to find a list of Tolvon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tolvon CEP of the European Pharmacopoeia monograph is often referred to as a Tolvon Certificate of Suitability (COS). The purpose of a Tolvon CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tolvon EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tolvon to their clients by showing that a Tolvon CEP has been issued for it. The manufacturer submits a Tolvon CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tolvon CEP holder for the record. Additionally, the data presented in the Tolvon CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tolvon DMF.
A Tolvon CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tolvon 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 Tolvon suppliers with CEP (COS) on PharmaCompass.