Synthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
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01 1SYNTHOKEM LABS PRIVATE LIMITED Hyderabad IN
02 1COHANCE LIFESCIENCES LIMITED Hyderabad IN
03 1PIRAMAL PHARMA LIMITED Digwal Village IN
04 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S.P.A. Milano IT
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01 4Mebeverine hydrochloride
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01 2India
02 1Italy
03 1U.S.A
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01 4Valid
Certificate Number : CEP 2021-271 - Rev 00
Status : Valid
Issue Date : 2023-09-25
Type : Chemical
Substance Number : 2097
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Certificate Number : R0-CEP 2019-061 - Rev 02
Status : Valid
Issue Date : 2022-12-15
Type : Chemical
Substance Number : 2097
Certificate Number : R0-CEP 2019-271 - Rev 03
Status : Valid
Issue Date : 2022-01-07
Type : Chemical
Substance Number : 2097
Certificate Number : CEP 2022-002 - Rev 00
Status : Valid
Issue Date : 2024-03-13
Type : Chemical
Substance Number : 2097
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PharmaCompass offers a list of Mebeverine 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 Mebeverine manufacturer or Mebeverine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mebeverine manufacturer or Mebeverine supplier.
PharmaCompass also assists you with knowing the Mebeverine API Price utilized in the formulation of products. Mebeverine API Price is not always fixed or binding as the Mebeverine Price is obtained through a variety of data sources. The Mebeverine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Duspatal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Duspatal, including repackagers and relabelers. The FDA regulates Duspatal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Duspatal 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 Duspatal manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Duspatal supplier is an individual or a company that provides Duspatal active pharmaceutical ingredient (API) or Duspatal finished formulations upon request. The Duspatal suppliers may include Duspatal API manufacturers, exporters, distributors and traders.
click here to find a list of Duspatal suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Duspatal CEP of the European Pharmacopoeia monograph is often referred to as a Duspatal Certificate of Suitability (COS). The purpose of a Duspatal CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Duspatal EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Duspatal to their clients by showing that a Duspatal CEP has been issued for it. The manufacturer submits a Duspatal CEP (COS) as part of the market authorization procedure, and it takes on the role of a Duspatal CEP holder for the record. Additionally, the data presented in the Duspatal CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Duspatal DMF.
A Duspatal CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Duspatal 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 Duspatal suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering Duspatal
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