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Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards. 
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01 TRANSO-PHARM HANDELS GMBH Siek DE (1)
02 Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Am Rhein DE (1)
03 Cambrex Profarmaco Milano S.r.l. Paullo IT (1)
04 MEDINEX LABORATORIES PRIVATE LIMITED Mumbai IN (1)
05 MYLAN LABORATORIES LIMITED Hyderabad IN (1)
06 ROUVER INVESTMENT S.A.R.L. Luxembourg LU (1)
07 WUHAN WUYAO PHARMACEUTICAL CO., LTD. Huangshi City CN (1)
01 Adrenaline tartrate (7)
01 China (1)
02 Germany (2)
03 India (1)
04 Luxembourg (1)
05 U.S.A (2)
01 Expired (1)
02 Valid (4)
03 Withdrawn by EDQM Failure to CEP procedure (1)
04 Withdrawn by Holder (1)
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PharmaCompass offers a list of Epinephrine Bitartrate 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 Epinephrine Bitartrate manufacturer or Epinephrine Bitartrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Epinephrine Bitartrate manufacturer or Epinephrine Bitartrate supplier.
PharmaCompass also assists you with knowing the Epinephrine Bitartrate API Price utilized in the formulation of products. Epinephrine Bitartrate API Price is not always fixed or binding as the Epinephrine Bitartrate Price is obtained through a variety of data sources. The Epinephrine Bitartrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_202839 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202839, including repackagers and relabelers. The FDA regulates Tox21_202839 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202839 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_202839 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tox21_202839 supplier is an individual or a company that provides Tox21_202839 active pharmaceutical ingredient (API) or Tox21_202839 finished formulations upon request. The Tox21_202839 suppliers may include Tox21_202839 API manufacturers, exporters, distributors and traders.
click here to find a list of Tox21_202839 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tox21_202839 CEP of the European Pharmacopoeia monograph is often referred to as a Tox21_202839 Certificate of Suitability (COS). The purpose of a Tox21_202839 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tox21_202839 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tox21_202839 to their clients by showing that a Tox21_202839 CEP has been issued for it. The manufacturer submits a Tox21_202839 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tox21_202839 CEP holder for the record. Additionally, the data presented in the Tox21_202839 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tox21_202839 DMF.
A Tox21_202839 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tox21_202839 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_202839 suppliers with CEP (COS) on PharmaCompass.
We have 6 companies offering Tox21_202839
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