Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
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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
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01 7Tolterodine tartrate
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01 4India
02 1Poland
03 2Spain
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01 7Valid
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
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.
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
Certificate Number : CEP 2015-020 - Rev 01
Status : Valid
Issue Date : 2023-12-06
Type : Chemical
Substance Number : 2781
Certificate Number : CEP 2020-032 - Rev 01
Status : Valid
Issue Date : 2025-04-25
Type : Chemical
Substance Number : 2781
Certificate Number : R1-CEP 2017-007 - Rev 00
Status : Valid
Issue Date : 2023-05-25
Type : Chemical
Substance Number : 2781
Certificate Number : R0-CEP 2021-020 - Rev 01
Status : Valid
Issue Date : 2023-02-15
Type : Chemical
Substance Number : 2781
Certificate Number : CEP 2021-381 - Rev 00
Status : Valid
Issue Date : 2023-10-13
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 CS-0441 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CS-0441, including repackagers and relabelers. The FDA regulates CS-0441 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CS-0441 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 CS-0441 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CS-0441 supplier is an individual or a company that provides CS-0441 active pharmaceutical ingredient (API) or CS-0441 finished formulations upon request. The CS-0441 suppliers may include CS-0441 API manufacturers, exporters, distributors and traders.
click here to find a list of CS-0441 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CS-0441 CEP of the European Pharmacopoeia monograph is often referred to as a CS-0441 Certificate of Suitability (COS). The purpose of a CS-0441 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CS-0441 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CS-0441 to their clients by showing that a CS-0441 CEP has been issued for it. The manufacturer submits a CS-0441 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CS-0441 CEP holder for the record. Additionally, the data presented in the CS-0441 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CS-0441 DMF.
A CS-0441 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CS-0441 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 CS-0441 suppliers with CEP (COS) on PharmaCompass.
We have 7 companies offering CS-0441
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