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Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs. 
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01 SYMBIOTEC PHARMALAB PRIVATE LIMITED Indore IN (1)
02 ASPEN OSS B.V. Oss NL (1)
03 BAYER AG Leverkusen DE (1)
04 GEDEON RICHTER PLC Budapest HU (1)
05 Industriale Chimica S.R.L. Saronno IT (1)
06 Jenapharm GmbH & Co KG Jena DE (1)
07 LUPIN LIMITED Mumbai IN (1)
08 QINHUANGDAO ZIZHU PHARMACEUTICAL CO., LTD. Qinhuangdao City CN (1)
09 VALDEPHARM Val De Reuil FR (1)
10 ZHEJIANG XIANJU PHARMACEUTICAL CO., LTD. Xianju CN (2)
01 Ethinylestradiol (7)
02 Ethinylestradiol, Micronised (2)
03 Ethinylestradiol, Micronised, non-micronised (1)
04 Ethinylestradiol, micronized, non micronized (1)
01 China (3)
02 France (1)
03 Germany (2)
04 Hungary (1)
05 India (2)
06 Italy (1)
07 Netherlands (1)
01 Valid (9)
02 Withdrawn by EDQM Failure to CEP procedure (1)
03 Withdrawn by Holder (1)
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PharmaCompass offers a list of Ethinyl Estradiol 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 Ethinyl Estradiol manufacturer or Ethinyl Estradiol supplier for your needs.
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PharmaCompass also assists you with knowing the Ethinyl Estradiol API Price utilized in the formulation of products. Ethinyl Estradiol API Price is not always fixed or binding as the Ethinyl Estradiol Price is obtained through a variety of data sources. The Ethinyl Estradiol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_300413 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300413, including repackagers and relabelers. The FDA regulates Tox21_300413 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300413 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 Tox21_300413 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tox21_300413 supplier is an individual or a company that provides Tox21_300413 active pharmaceutical ingredient (API) or Tox21_300413 finished formulations upon request. The Tox21_300413 suppliers may include Tox21_300413 API manufacturers, exporters, distributors and traders.
click here to find a list of Tox21_300413 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tox21_300413 CEP of the European Pharmacopoeia monograph is often referred to as a Tox21_300413 Certificate of Suitability (COS). The purpose of a Tox21_300413 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tox21_300413 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tox21_300413 to their clients by showing that a Tox21_300413 CEP has been issued for it. The manufacturer submits a Tox21_300413 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tox21_300413 CEP holder for the record. Additionally, the data presented in the Tox21_300413 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tox21_300413 DMF.
A Tox21_300413 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tox21_300413 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 Tox21_300413 suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering Tox21_300413
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