01 1AARTI DRUGS LIMITED Mumbai IN
01 1Tolnaftate
01 1India
01 1Withdrawn by Holder
Certificate Number : R1-CEP 2002-087 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2009-11-25
Type : Chemical
Substance Number : 1158
32
PharmaCompass offers a list of Tolnaftate 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 Tolnaftate manufacturer or Tolnaftate supplier for your needs.
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PharmaCompass also assists you with knowing the Tolnaftate API Price utilized in the formulation of products. Tolnaftate API Price is not always fixed or binding as the Tolnaftate Price is obtained through a variety of data sources. The Tolnaftate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sporiline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sporiline, including repackagers and relabelers. The FDA regulates Sporiline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sporiline API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Sporiline supplier is an individual or a company that provides Sporiline active pharmaceutical ingredient (API) or Sporiline finished formulations upon request. The Sporiline suppliers may include Sporiline API manufacturers, exporters, distributors and traders.
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A Sporiline CEP of the European Pharmacopoeia monograph is often referred to as a Sporiline Certificate of Suitability (COS). The purpose of a Sporiline CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sporiline EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sporiline to their clients by showing that a Sporiline CEP has been issued for it. The manufacturer submits a Sporiline CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sporiline CEP holder for the record. Additionally, the data presented in the Sporiline CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sporiline DMF.
A Sporiline CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sporiline CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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