01 1ABC Farmaceutici S.p.A. Ivrea IT
02 1ELIXIR PHARMA Ahmedabad IN
03 1UNIMARK REMEDIES LIMITED Mumbai IN
01 3Nalidixic Acid - Text Deleted 1/01/2021
01 2India
02 1Italy
01 1Expired
02 2Withdrawn by EDQM Failure to CEP procedure
Nalidixic Acid - Text Deleted 1/01/2021
Certificate Number : R1-CEP 2009-216 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2016-02-24
Type : Chemical
Substance Number : 701
Nalidixic Acid - Text Deleted 1/01/2021
Certificate Number : R0-CEP 2012-005 - Rev 01
Status : Expired
Issue Date : 2016-08-05
Type : Chemical
Substance Number : 701
Nalidixic Acid - Text Deleted 1/01/2021
Certificate Number : R1-CEP 2011-088 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2016-06-17
Type : Chemical
Substance Number : 701
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PharmaCompass offers a list of Nalidixic Acid 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 Nalidixic Acid manufacturer or Nalidixic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nalidixic Acid manufacturer or Nalidixic Acid supplier.
PharmaCompass also assists you with knowing the Nalidixic Acid API Price utilized in the formulation of products. Nalidixic Acid API Price is not always fixed or binding as the Nalidixic Acid Price is obtained through a variety of data sources. The Nalidixic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Uralgin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Uralgin, including repackagers and relabelers. The FDA regulates Uralgin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Uralgin 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 Uralgin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Uralgin supplier is an individual or a company that provides Uralgin active pharmaceutical ingredient (API) or Uralgin finished formulations upon request. The Uralgin suppliers may include Uralgin API manufacturers, exporters, distributors and traders.
click here to find a list of Uralgin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Uralgin CEP of the European Pharmacopoeia monograph is often referred to as a Uralgin Certificate of Suitability (COS). The purpose of a Uralgin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Uralgin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Uralgin to their clients by showing that a Uralgin CEP has been issued for it. The manufacturer submits a Uralgin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Uralgin CEP holder for the record. Additionally, the data presented in the Uralgin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Uralgin DMF.
A Uralgin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Uralgin 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 Uralgin suppliers with CEP (COS) on PharmaCompass.
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