01 1APICORE US LLC Somerset US
02 1EMCURE PHARMACEUTICALS LIMITED Pune IN
03 1EXCELLA GMBH & CO. KG Feucht DE
04 1FRESENIUS KABI ONCOLOGY LIMITED Kalyani IN
05 1SHILPA PHARMA LIFESCIENCES LIMITED Raichur IN
06 1SHIVALIK RASAYAN LIMITED New Delhi IN
01 6Busulfan
01 1Germany
02 4India
03 1U.S.A
01 6Valid
Certificate Number : R1-CEP 2016-270 - Rev 00
Status : Valid
Issue Date : 2023-05-17
Type : Chemical
Substance Number : 542
Certificate Number : R1-CEP 2013-341 - Rev 01
Status : Valid
Issue Date : 2023-08-31
Type : Chemical
Substance Number : 542
Certificate Number : R1-CEP 2013-212 - Rev 00
Status : Valid
Issue Date : 2020-04-28
Type : Chemical
Substance Number : 542
Certificate Number : CEP 2010-374 - Rev 08
Status : Valid
Issue Date : 2025-02-03
Type : Chemical
Substance Number : 542
Certificate Number : R1-CEP 2011-339 - Rev 02
Status : Valid
Issue Date : 2022-07-20
Type : Chemical
Substance Number : 542
Certificate Number : R0-CEP 2021-356 - Rev 00
Status : Valid
Issue Date : 2022-12-01
Type : Chemical
Substance Number : 542
78
PharmaCompass offers a list of Busulfan 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 Busulfan manufacturer or Busulfan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Busulfan manufacturer or Busulfan supplier.
PharmaCompass also assists you with knowing the Busulfan API Price utilized in the formulation of products. Busulfan API Price is not always fixed or binding as the Busulfan Price is obtained through a variety of data sources. The Busulfan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Busilvex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Busilvex, including repackagers and relabelers. The FDA regulates Busilvex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Busilvex 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 Busilvex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Busilvex supplier is an individual or a company that provides Busilvex active pharmaceutical ingredient (API) or Busilvex finished formulations upon request. The Busilvex suppliers may include Busilvex API manufacturers, exporters, distributors and traders.
click here to find a list of Busilvex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Busilvex CEP of the European Pharmacopoeia monograph is often referred to as a Busilvex Certificate of Suitability (COS). The purpose of a Busilvex CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Busilvex EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Busilvex to their clients by showing that a Busilvex CEP has been issued for it. The manufacturer submits a Busilvex CEP (COS) as part of the market authorization procedure, and it takes on the role of a Busilvex CEP holder for the record. Additionally, the data presented in the Busilvex CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Busilvex DMF.
A Busilvex CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Busilvex 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 Busilvex suppliers with CEP (COS) on PharmaCompass.
We have 6 companies offering Busilvex
Get in contact with the supplier of your choice:
