LEBSA- Your strategic API source for niche molecules.
01 1Laboratorios Espinos Y Bofill S.A. (LEBSA) Cornellà ES
02 1ARCHIMICA S.P.A Lodi IT
03 1EXCELLA GMBH & CO. KG Feucht DE
01 2Mianserin hydrochloride
02 1Mianserin hydrochloride, Process II
01 1Germany
02 1Italy
03 1Spain
01 3Valid
LEBSA- Your strategic API source for niche molecules.
LEBSA- Your strategic API source for niche molecules.
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
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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 Lerivon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lerivon, including repackagers and relabelers. The FDA regulates Lerivon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lerivon 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 Lerivon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lerivon supplier is an individual or a company that provides Lerivon active pharmaceutical ingredient (API) or Lerivon finished formulations upon request. The Lerivon suppliers may include Lerivon API manufacturers, exporters, distributors and traders.
click here to find a list of Lerivon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lerivon CEP of the European Pharmacopoeia monograph is often referred to as a Lerivon Certificate of Suitability (COS). The purpose of a Lerivon CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lerivon EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lerivon to their clients by showing that a Lerivon CEP has been issued for it. The manufacturer submits a Lerivon CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lerivon CEP holder for the record. Additionally, the data presented in the Lerivon CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lerivon DMF.
A Lerivon CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lerivon 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 Lerivon suppliers with CEP (COS) on PharmaCompass.
