With Fermion, start the journey of your innovative API.
01 1FERMION OY Espoo FI
02 1MAITHRI LABORATORIES PRIVATE LIMITED Gaddapotharam Village IN
03 1SOLARA ACTIVE PHARMA SCIENCES LIMITED Chennai IN
04 1UNIMARK REMEDIES LIMITED Mumbai IN
05 1Unichem Laboratories Limited Mumbai IN
01 5Buspirone hydrochloride
01 1Finland
02 4India
01 1Expired
02 4Valid
With Fermion, start the journey of your innovative API.
With Fermion, start the journey of your innovative API.
Certificate Number : R0-CEP 2021-262 - Rev 00
Status : Valid
Issue Date : 2022-10-27
Type : Chemical
Substance Number : 1711
Certificate Number : CEP 2023-395 - Rev 00
Status : Valid
Issue Date : 2025-02-12
Type : Chemical
Substance Number : 1711
Certificate Number : CEP 2021-174 - Rev 01
Status : Valid
Issue Date : 2024-05-24
Type : Chemical
Substance Number : 1711
Certificate Number : CEP 2022-151 - Rev 01
Status : Valid
Issue Date : 2024-11-05
Type : Chemical
Substance Number : 1711
Certificate Number : R0-CEP 2012-361 - Rev 00
Status : Expired
Issue Date : 2014-11-13
Type : Chemical
Substance Number : 1711
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PharmaCompass offers a list of Buspirone 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 Buspirone Hydrochloride manufacturer or Buspirone Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Buspirone Hydrochloride manufacturer or Buspirone Hydrochloride supplier.
PharmaCompass also assists you with knowing the Buspirone Hydrochloride API Price utilized in the formulation of products. Buspirone Hydrochloride API Price is not always fixed or binding as the Buspirone Hydrochloride Price is obtained through a variety of data sources. The Buspirone Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Anxut manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anxut, including repackagers and relabelers. The FDA regulates Anxut manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anxut 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 Anxut manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Anxut supplier is an individual or a company that provides Anxut active pharmaceutical ingredient (API) or Anxut finished formulations upon request. The Anxut suppliers may include Anxut API manufacturers, exporters, distributors and traders.
click here to find a list of Anxut suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Anxut CEP of the European Pharmacopoeia monograph is often referred to as a Anxut Certificate of Suitability (COS). The purpose of a Anxut CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Anxut EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Anxut to their clients by showing that a Anxut CEP has been issued for it. The manufacturer submits a Anxut CEP (COS) as part of the market authorization procedure, and it takes on the role of a Anxut CEP holder for the record. Additionally, the data presented in the Anxut CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Anxut DMF.
A Anxut CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Anxut 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 Anxut suppliers with CEP (COS) on PharmaCompass.
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