Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
01 1Interquim, S.A. Sant Cugat Del Vallès ES
02 2DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
03 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
04 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
05 1CAMBREX KARLSKOGA AB Karlskoga SE
06 1CIPLA LIMITED Mumbai IN
07 1MSN ORGANICS PRIVATE LIMITED Bibinagar Village IN
08 2SANECA PHARMACEUTICALS A.S. Hlohovec SK
09 1SHODHANA LABORATORIES LIMITED Hyderabad IN
10 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
Rivastigmine Hydrogen Tartrate
Certificate Number : R1-CEP 2013-331 - Rev 00
Status : Valid
Issue Date : 2020-01-23
Type : Chemical
Substance Number : 2630
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Rivastigmine Hydrogen Tartrate
Certificate Number : R1-CEP 2013-305 - Rev 00
Status : Valid
Issue Date : 2020-01-13
Type : Chemical
Substance Number : 2630
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Rivastigmine Hydrogen Tartrate, Process – I
Certificate Number : R0-CEP 2021-248 - Rev 00
Status : Valid
Issue Date : 2021-12-09
Type : Chemical
Substance Number : 2630
A Rivastigmine Tartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rivastigmine Tartrate, including repackagers and relabelers. The FDA regulates Rivastigmine Tartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rivastigmine Tartrate 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 Rivastigmine Tartrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rivastigmine Tartrate supplier is an individual or a company that provides Rivastigmine Tartrate active pharmaceutical ingredient (API) or Rivastigmine Tartrate finished formulations upon request. The Rivastigmine Tartrate suppliers may include Rivastigmine Tartrate API manufacturers, exporters, distributors and traders.
click here to find a list of Rivastigmine Tartrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Rivastigmine Tartrate CEP of the European Pharmacopoeia monograph is often referred to as a Rivastigmine Tartrate Certificate of Suitability (COS). The purpose of a Rivastigmine Tartrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Rivastigmine Tartrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Rivastigmine Tartrate to their clients by showing that a Rivastigmine Tartrate CEP has been issued for it. The manufacturer submits a Rivastigmine Tartrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Rivastigmine Tartrate CEP holder for the record. Additionally, the data presented in the Rivastigmine Tartrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Rivastigmine Tartrate DMF.
A Rivastigmine Tartrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Rivastigmine Tartrate 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 Rivastigmine Tartrate suppliers with CEP (COS) on PharmaCompass.
We have 10 companies offering Rivastigmine Tartrate
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