Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
01 1EGIS Pharmaceuticals PLC Budapest HU
02 1Sanofi Winthrop Industrie Gentilly FR
03 1BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. Hyderabad IN
04 1MAITHRI LABORATORIES PRIVATE LIMITED Gaddapotharam Village IN
05 1R L FINE CHEM PVT. LTD. Gowribidanur IN
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Certificate Number : R1-CEP 1996-077 - Rev 07
Status : Valid
Issue Date : 2021-10-15
Type : Chemical
Substance Number : 475
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Certificate Number : CEP 1999-043 - Rev 08
Status : Valid
Issue Date : 2024-02-16
Type : Chemical
Substance Number : 475
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Certificate Number : R0-CEP 2021-266 - Rev 00
Status : Valid
Issue Date : 2023-03-08
Type : Chemical
Substance Number : 475
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PharmaCompass offers a list of Chlorpromazine Hydrochloride 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 Chlorpromazine Hydrochloride manufacturer or Chlorpromazine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Chlorpromazine Hydrochloride API Price utilized in the formulation of products. Chlorpromazine Hydrochloride API Price is not always fixed or binding as the Chlorpromazine Hydrochloride Price is obtained through a variety of data sources. The Chlorpromazine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_300517 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300517, including repackagers and relabelers. The FDA regulates Tox21_300517 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300517 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tox21_300517 supplier is an individual or a company that provides Tox21_300517 active pharmaceutical ingredient (API) or Tox21_300517 finished formulations upon request. The Tox21_300517 suppliers may include Tox21_300517 API manufacturers, exporters, distributors and traders.
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A Tox21_300517 CEP of the European Pharmacopoeia monograph is often referred to as a Tox21_300517 Certificate of Suitability (COS). The purpose of a Tox21_300517 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tox21_300517 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tox21_300517 to their clients by showing that a Tox21_300517 CEP has been issued for it. The manufacturer submits a Tox21_300517 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tox21_300517 CEP holder for the record. Additionally, the data presented in the Tox21_300517 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tox21_300517 DMF.
A Tox21_300517 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tox21_300517 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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We have 5 companies offering Tox21_300517
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