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 C.B. 2041 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C.B. 2041, including repackagers and relabelers. The FDA regulates C.B. 2041 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C.B. 2041 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 C.B. 2041 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A C.B. 2041 supplier is an individual or a company that provides C.B. 2041 active pharmaceutical ingredient (API) or C.B. 2041 finished formulations upon request. The C.B. 2041 suppliers may include C.B. 2041 API manufacturers, exporters, distributors and traders.
click here to find a list of C.B. 2041 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A C.B. 2041 CEP of the European Pharmacopoeia monograph is often referred to as a C.B. 2041 Certificate of Suitability (COS). The purpose of a C.B. 2041 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of C.B. 2041 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of C.B. 2041 to their clients by showing that a C.B. 2041 CEP has been issued for it. The manufacturer submits a C.B. 2041 CEP (COS) as part of the market authorization procedure, and it takes on the role of a C.B. 2041 CEP holder for the record. Additionally, the data presented in the C.B. 2041 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the C.B. 2041 DMF.
A C.B. 2041 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. C.B. 2041 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 C.B. 2041 suppliers with CEP (COS) on PharmaCompass.
We have 6 companies offering C.B. 2041
Get in contact with the supplier of your choice:
