01 1Fersinsa GB S.A. De C.V. Ramos Arizpe MX
02 1INNER MONGOLIA CHANGSHENG PHARMACEUTICAL CO., LTD. Tuoketuo CN
03 1PARABOLIC DRUGS LIMITED Panchkula District IN
04 1Sandoz Industrial Products S.A. Les Franqueses Del Vallès ES
01 2Ampicillin
02 1Ampicillin, Mexico
03 1Ampicillin, Powder, compacted
01 1China
02 1Germany
03 1India
04 1Netherlands
01 3Valid
02 1Withdrawn by EDQM Failure to CEP procedure
Certificate Number : CEP 2024-308 - Rev 00
Status : Valid
Issue Date : 2025-02-19
Type : Chemical
Substance Number : 167
Certificate Number : R0-CEP 2011-090 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2013-03-07
Type : Chemical
Substance Number : 167
Certificate Number : R2-CEP 1995-031 - Rev 05
Status : Valid
Issue Date : 2022-02-21
Type : Chemical
Substance Number : 167
Certificate Number : R1-CEP 1999-188 - Rev 03
Status : Valid
Issue Date : 2018-01-15
Type : Chemical
Substance Number : 167
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PharmaCompass offers a list of Ampicillin 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 Ampicillin manufacturer or Ampicillin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ampicillin manufacturer or Ampicillin supplier.
PharmaCompass also assists you with knowing the Ampicillin API Price utilized in the formulation of products. Ampicillin API Price is not always fixed or binding as the Ampicillin Price is obtained through a variety of data sources. The Ampicillin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Trifacilina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trifacilina, including repackagers and relabelers. The FDA regulates Trifacilina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trifacilina 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 Trifacilina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trifacilina supplier is an individual or a company that provides Trifacilina active pharmaceutical ingredient (API) or Trifacilina finished formulations upon request. The Trifacilina suppliers may include Trifacilina API manufacturers, exporters, distributors and traders.
click here to find a list of Trifacilina suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Trifacilina CEP of the European Pharmacopoeia monograph is often referred to as a Trifacilina Certificate of Suitability (COS). The purpose of a Trifacilina CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Trifacilina EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Trifacilina to their clients by showing that a Trifacilina CEP has been issued for it. The manufacturer submits a Trifacilina CEP (COS) as part of the market authorization procedure, and it takes on the role of a Trifacilina CEP holder for the record. Additionally, the data presented in the Trifacilina CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Trifacilina DMF.
A Trifacilina CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Trifacilina 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 Trifacilina suppliers with CEP (COS) on PharmaCompass.
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