01 CHEMI S.P.A. Patrica IT (1)
02 DIVI'S LABORATORIES LIMITED Hyderabad IN (1)
03 IPCA Laboratories Limited Mumbai IN (1)
04 MYLAN LABORATORIES LIMITED Hyderabad IN (1)
05 TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL (1)
01 Nabumetone (4)
02 Nabumetone, FV 4074 (1)
01 India (2)
02 Israel (1)
03 Italy (1)
04 U.S.A (1)
01 Valid (4)
02 Withdrawn by Holder (1)
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PharmaCompass offers a list of Nabumetone 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 Nabumetone manufacturer or Nabumetone supplier for your needs.
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PharmaCompass also assists you with knowing the Nabumetone API Price utilized in the formulation of products. Nabumetone API Price is not always fixed or binding as the Nabumetone Price is obtained through a variety of data sources. The Nabumetone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MolPort-001-793-710 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-793-710, including repackagers and relabelers. The FDA regulates MolPort-001-793-710 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-793-710 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 MolPort-001-793-710 supplier is an individual or a company that provides MolPort-001-793-710 active pharmaceutical ingredient (API) or MolPort-001-793-710 finished formulations upon request. The MolPort-001-793-710 suppliers may include MolPort-001-793-710 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-793-710 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MolPort-001-793-710 CEP of the European Pharmacopoeia monograph is often referred to as a MolPort-001-793-710 Certificate of Suitability (COS). The purpose of a MolPort-001-793-710 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MolPort-001-793-710 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MolPort-001-793-710 to their clients by showing that a MolPort-001-793-710 CEP has been issued for it. The manufacturer submits a MolPort-001-793-710 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MolPort-001-793-710 CEP holder for the record. Additionally, the data presented in the MolPort-001-793-710 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MolPort-001-793-710 DMF.
A MolPort-001-793-710 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MolPort-001-793-710 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 MolPort-001-793-710 suppliers with CEP (COS) on PharmaCompass.
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