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 1PHARMACEUTICAL WORKS POLPHARMA S.A. Starogard Gdanski PL
03 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 1HETERO DRUGS LIMITED Hyderabad IN
05 1MACLEODS PHARMACEUTICALS LIMITED Mumbai IN
06 1MAITHRI LABORATORIES PRIVATE LIMITED Gaddapotharam Village IN
07 1Uquifa Mexico S.A. de C.V. Jiutepec MX
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
Certificate Number : R1-CEP 2015-301 - Rev 01
Status : Valid
Issue Date : 2022-07-18
Type : Chemical
Substance Number : 2781
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Certificate Number : R1-CEP 2015-192 - Rev 00
Status : Valid
Issue Date : 2021-08-30
Type : Chemical
Substance Number : 2781
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PharmaCompass offers a list of Tolterodine Tartrate 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 Tolterodine Tartrate manufacturer or Tolterodine Tartrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tolterodine Tartrate manufacturer or Tolterodine Tartrate supplier.
PharmaCompass also assists you with knowing the Tolterodine Tartrate API Price utilized in the formulation of products. Tolterodine Tartrate API Price is not always fixed or binding as the Tolterodine Tartrate Price is obtained through a variety of data sources. The Tolterodine Tartrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Urotrol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Urotrol, including repackagers and relabelers. The FDA regulates Urotrol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Urotrol 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 Urotrol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Urotrol supplier is an individual or a company that provides Urotrol active pharmaceutical ingredient (API) or Urotrol finished formulations upon request. The Urotrol suppliers may include Urotrol API manufacturers, exporters, distributors and traders.
click here to find a list of Urotrol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Urotrol CEP of the European Pharmacopoeia monograph is often referred to as a Urotrol Certificate of Suitability (COS). The purpose of a Urotrol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Urotrol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Urotrol to their clients by showing that a Urotrol CEP has been issued for it. The manufacturer submits a Urotrol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Urotrol CEP holder for the record. Additionally, the data presented in the Urotrol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Urotrol DMF.
A Urotrol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Urotrol 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 Urotrol suppliers with CEP (COS) on PharmaCompass.
We have 7 companies offering Urotrol
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