Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
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01 2SANOFI-AVENTIS DEUTSCHLAND GMBH Frankfurt am Main DE
02 1RUSAN PHARMA LTD Mumbai IN
03 1EMBIO LIMITED Powai, Mumbai IN
04 1HARMAN FINOCHEM LIMITED Mumbai IN
05 1MACFARLAN SMITH LIMITED Edinburgh GB
06 1PIONEER AGRO INDUSTRIES SANVIN LABORATORIES PRIVATE LIMITED Mumbai IN
07 1SANECA PHARMACEUTICALS A.S. Hlohovec SK
08 1SIEGFRIED LTD. Zofingen CH
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01 8Methadone hydrochloride
02 1Methadone hydrochloride, Alternative grade
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01 2Germany
02 4India
03 1Slovakia
04 1Switzerland
05 1United Kingdom
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01 7Valid
02 2Withdrawn by Holder
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Certificate Number : R0-CEP 2012-206 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2015-05-18
Type : Chemical
Substance Number : 408
Certificate Number : CEP 2017-277 - Rev 03
Status : Valid
Issue Date : 2024-05-30
Type : Chemical
Substance Number : 408
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Methadone Hydrochloride, Alternative Grade
Certificate Number : R0-CEP 2015-358 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2016-05-24
Type : Chemical
Substance Number : 408
Certificate Number : R0-CEP 2020-306 - Rev 00
Status : Valid
Issue Date : 2022-05-06
Type : Chemical
Substance Number : 408
Certificate Number : CEP 2011-086 - Rev 01
Status : Valid
Issue Date : 2025-04-16
Type : Chemical
Substance Number : 408
Certificate Number : CEP 2003-062 - Rev 01
Status : Valid
Issue Date : 2023-10-03
Type : Chemical
Substance Number : 408
Certificate Number : R1-CEP 2007-068 - Rev 01
Status : Valid
Issue Date : 2018-09-07
Type : Chemical
Substance Number : 408
Certificate Number : R2-CEP 1995-043 - Rev 04
Status : Valid
Issue Date : 2019-08-05
Type : Chemical
Substance Number : 408
Certificate Number : R1-CEP 1999-182 - Rev 02
Status : Valid
Issue Date : 2008-11-25
Type : Chemical
Substance Number : 408
44
PharmaCompass offers a list of Methadone 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 Methadone Hydrochloride manufacturer or Methadone Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Methadone Hydrochloride API Price utilized in the formulation of products. Methadone Hydrochloride API Price is not always fixed or binding as the Methadone Hydrochloride Price is obtained through a variety of data sources. The Methadone Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Butalgin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Butalgin, including repackagers and relabelers. The FDA regulates Butalgin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Butalgin 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 Butalgin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Butalgin supplier is an individual or a company that provides Butalgin active pharmaceutical ingredient (API) or Butalgin finished formulations upon request. The Butalgin suppliers may include Butalgin API manufacturers, exporters, distributors and traders.
click here to find a list of Butalgin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Butalgin CEP of the European Pharmacopoeia monograph is often referred to as a Butalgin Certificate of Suitability (COS). The purpose of a Butalgin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Butalgin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Butalgin to their clients by showing that a Butalgin CEP has been issued for it. The manufacturer submits a Butalgin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Butalgin CEP holder for the record. Additionally, the data presented in the Butalgin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Butalgin DMF.
A Butalgin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Butalgin 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 Butalgin suppliers with CEP (COS) on PharmaCompass.
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