01 2ABBOTT LABORATORIES Abbott Park US
02 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
03 1LUPIN LIMITED Mumbai IN
04 1ROLABO OUTSOURCING, S.L. Zaragoza ES
05 1VITALIFE LABORATORIES Mumbai IN
01 6Trandolapril
01 3India
02 1Spain
03 2U.S.A
01 5Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2009-182 - Rev 01
Status : Valid
Issue Date : 2020-03-13
Type : Chemical
Substance Number : 2245
Certificate Number : R0-CEP 2019-137 - Rev 01
Status : Valid
Issue Date : 2022-09-08
Type : Chemical
Substance Number : 2245
Certificate Number : R1-CEP 2007-287 - Rev 02
Status : Valid
Issue Date : 2020-02-05
Type : Chemical
Substance Number : 2245
Certificate Number : CEP 2007-184 - Rev 06
Status : Valid
Issue Date : 2023-11-16
Type : Chemical
Substance Number : 2245
Certificate Number : R1-CEP 2009-099 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2019-06-25
Type : Chemical
Substance Number : 2245
Certificate Number : R1-CEP 2009-251 - Rev 01
Status : Valid
Issue Date : 2019-12-16
Type : Chemical
Substance Number : 2245
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PharmaCompass offers a list of Trandolapril 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 Trandolapril manufacturer or Trandolapril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trandolapril manufacturer or Trandolapril supplier.
PharmaCompass also assists you with knowing the Trandolapril API Price utilized in the formulation of products. Trandolapril API Price is not always fixed or binding as the Trandolapril Price is obtained through a variety of data sources. The Trandolapril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Udrik manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Udrik, including repackagers and relabelers. The FDA regulates Udrik manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Udrik 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 Udrik manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Udrik supplier is an individual or a company that provides Udrik active pharmaceutical ingredient (API) or Udrik finished formulations upon request. The Udrik suppliers may include Udrik API manufacturers, exporters, distributors and traders.
click here to find a list of Udrik suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Udrik CEP of the European Pharmacopoeia monograph is often referred to as a Udrik Certificate of Suitability (COS). The purpose of a Udrik CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Udrik EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Udrik to their clients by showing that a Udrik CEP has been issued for it. The manufacturer submits a Udrik CEP (COS) as part of the market authorization procedure, and it takes on the role of a Udrik CEP holder for the record. Additionally, the data presented in the Udrik CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Udrik DMF.
A Udrik CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Udrik 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 Udrik suppliers with CEP (COS) on PharmaCompass.
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