With Fermion, start the journey of your innovative API.
01 1FERMION OY Espoo FI
02 1SOLARA ACTIVE PHARMA SCIENCES LIMITED Chennai IN
03 1UNIMARK REMEDIES LIMITED Mumbai IN
04 1Unichem Laboratories Limited Mumbai IN
01 4Buspirone hydrochloride
01 1Finland
02 3India
01 1Expired
02 3Valid
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 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
A Buspirone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Buspirone Hydrochloride, including repackagers and relabelers. The FDA regulates Buspirone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Buspirone 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.
click here to find a list of Buspirone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Buspirone Hydrochloride supplier is an individual or a company that provides Buspirone Hydrochloride active pharmaceutical ingredient (API) or Buspirone Hydrochloride finished formulations upon request. The Buspirone Hydrochloride suppliers may include Buspirone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Buspirone Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Buspirone Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Buspirone Hydrochloride Certificate of Suitability (COS). The purpose of a Buspirone Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Buspirone Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Buspirone Hydrochloride to their clients by showing that a Buspirone Hydrochloride CEP has been issued for it. The manufacturer submits a Buspirone Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Buspirone Hydrochloride CEP holder for the record. Additionally, the data presented in the Buspirone Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Buspirone Hydrochloride DMF.
A Buspirone Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Buspirone 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 Buspirone Hydrochloride suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering Buspirone Hydrochloride
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