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Status : Withdrawn by EDQM Failure to CEP pro...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Status : Withdrawn by EDQM Failure to CEP pro...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 Urisal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Urisal, including repackagers and relabelers. The FDA regulates Urisal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Urisal 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 Urisal manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Urisal supplier is an individual or a company that provides Urisal active pharmaceutical ingredient (API) or Urisal finished formulations upon request. The Urisal suppliers may include Urisal API manufacturers, exporters, distributors and traders.
click here to find a list of Urisal suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Urisal CEP of the European Pharmacopoeia monograph is often referred to as a Urisal Certificate of Suitability (COS). The purpose of a Urisal CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Urisal EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Urisal to their clients by showing that a Urisal CEP has been issued for it. The manufacturer submits a Urisal CEP (COS) as part of the market authorization procedure, and it takes on the role of a Urisal CEP holder for the record. Additionally, the data presented in the Urisal CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Urisal DMF.
A Urisal CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Urisal 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 Urisal suppliers with CEP (COS) on PharmaCompass.
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