DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 2DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
02 1AUROBINDO PHARMA LIMITED Hyderabad IN
03 1Albemarle Corporation Orangeburg US
04 1CORDEN PHARMA BERGAMO S.P.A. Treviglio IT
05 1DIVI'S LABORATORIES LIMITED Hyderabad IN
06 1HY-GRO CHEMICALS PHARMTEK PRIVATE LIMITED Secunderabad IN
07 1MYLAN LABORATORIES LIMITED Hyderabad IN
08 1Pharmacin B.V. Zwijndrecht NL
09 1TAPI NL B.V. Amsterdam NL
10 1Zambon Group SpA Lonigo IT
11 1Zhejiang Charioteer Pharmaceutical Co., Ltd. Xianju CN
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Certificate Number : R1-CEP 1999-128 - Rev 07
Status : Valid
Issue Date : 2020-07-17
Type : Chemical
Substance Number : 731
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Certificate Number : R1-CEP 1997-039 - Rev 07
Status : Valid
Issue Date : 2019-06-21
Type : Chemical
Substance Number : 731
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PharmaCompass offers a list of Naproxen 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 Naproxen manufacturer or Naproxen supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Naproxen manufacturer or Naproxen supplier.
PharmaCompass also assists you with knowing the Naproxen API Price utilized in the formulation of products. Naproxen API Price is not always fixed or binding as the Naproxen Price is obtained through a variety of data sources. The Naproxen Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Naxen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Naxen, including repackagers and relabelers. The FDA regulates Naxen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Naxen 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 Naxen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Naxen supplier is an individual or a company that provides Naxen active pharmaceutical ingredient (API) or Naxen finished formulations upon request. The Naxen suppliers may include Naxen API manufacturers, exporters, distributors and traders.
click here to find a list of Naxen suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Naxen CEP of the European Pharmacopoeia monograph is often referred to as a Naxen Certificate of Suitability (COS). The purpose of a Naxen CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Naxen EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Naxen to their clients by showing that a Naxen CEP has been issued for it. The manufacturer submits a Naxen CEP (COS) as part of the market authorization procedure, and it takes on the role of a Naxen CEP holder for the record. Additionally, the data presented in the Naxen CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Naxen DMF.
A Naxen CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Naxen 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 Naxen suppliers with CEP (COS) on PharmaCompass.
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