Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
01 1ZHEJIANG HENGKANG PHARMACEUTICAL CO., LTD. Sanmen CN
02 1NEULAND LABORATORIES LIMITED Hyderabad IN
03 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
04 1ALIVUS LIFE SCIENCES LIMITED Mumbai IN
05 1AMOLI ORGANICS PRIVATE LIMITED Mumbai IN
06 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
07 1BIOCON LIMITED Bengaluru IN
08 1CTX LIFESCIENCES PVT. LIMITED Surat IN
09 1MSN LABORATORIES PRIVATE LIMITED Rudraram Village IN
10 1SYMED LABS LIMITED Hyderabad IN
11 1TAPI NL B.V. Amsterdam NL
12 1Ulkar Kimya Sanayii Ve Ticaret Anonim Sirketi Istanbul TR
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Certificate Number : CEP 2024-292 - Rev 00
Status : Valid
Issue Date : 2024-12-18
Type : Chemical
Substance Number : 2933
Neuland Laboratories- A dedicated 100% API provider.
Certificate Number : CEP 2020-280 - Rev 02
Status : Valid
Issue Date : 2024-03-20
Type : Chemical
Substance Number : 2933
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PharmaCompass offers a list of Deferasirox 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 Deferasirox manufacturer or Deferasirox supplier for your needs.
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A Exjade manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Exjade, including repackagers and relabelers. The FDA regulates Exjade manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Exjade 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 Exjade supplier is an individual or a company that provides Exjade active pharmaceutical ingredient (API) or Exjade finished formulations upon request. The Exjade suppliers may include Exjade API manufacturers, exporters, distributors and traders.
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A Exjade CEP of the European Pharmacopoeia monograph is often referred to as a Exjade Certificate of Suitability (COS). The purpose of a Exjade CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Exjade EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Exjade to their clients by showing that a Exjade CEP has been issued for it. The manufacturer submits a Exjade CEP (COS) as part of the market authorization procedure, and it takes on the role of a Exjade CEP holder for the record. Additionally, the data presented in the Exjade CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Exjade DMF.
A Exjade CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Exjade 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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