Neuland Laboratories- A dedicated 100% API provider.
01 1NEULAND LABORATORIES LIMITED Hyderabad IN
02 1AKTINOS PHARMA PRIVATE LIMITED Hyderabad IN
03 1Choongwae Pharma Corporation Seoul
04 1HETERO DRUGS LIMITED Hyderabad IN
05 2JANSSEN PHARMACEUTICA NV Beerse BE
06 1Janssen Pharmaceutical Ltd County Cork IE
07 1LEE PHARMA LIMITED Hyderabad IN
08 2NOSCH LABS PRIVATE LIMITED Hyderabad IN
09 2QUIMICA SINTETICA S.A. Alcala De Henares ES
10 2SMS PHARMACEUTICALS LIMITED Hyderabad IN
11 1STYRAX PHARMA PRIVATE LIMITED Visakhapatnam IN
12 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
13 1VASUDHA PHARMA CHEM LIMITED Hyderabad IN
14 1W. R. GRACE & CO.-CONN. Columbia US
Neuland Laboratories- A dedicated 100% API provider.
Certificate Number : R1-CEP 2003-220 - Rev 06
Status : Withdrawn by Holder
Issue Date : 2021-09-07
Type : Chemical
Substance Number : 1335
11
PharmaCompass offers a list of Itraconazole 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 Itraconazole manufacturer or Itraconazole supplier for your needs.
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A MolPort-000-883-864 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-000-883-864, including repackagers and relabelers. The FDA regulates MolPort-000-883-864 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-000-883-864 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-000-883-864 supplier is an individual or a company that provides MolPort-000-883-864 active pharmaceutical ingredient (API) or MolPort-000-883-864 finished formulations upon request. The MolPort-000-883-864 suppliers may include MolPort-000-883-864 API manufacturers, exporters, distributors and traders.
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A MolPort-000-883-864 CEP of the European Pharmacopoeia monograph is often referred to as a MolPort-000-883-864 Certificate of Suitability (COS). The purpose of a MolPort-000-883-864 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MolPort-000-883-864 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MolPort-000-883-864 to their clients by showing that a MolPort-000-883-864 CEP has been issued for it. The manufacturer submits a MolPort-000-883-864 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MolPort-000-883-864 CEP holder for the record. Additionally, the data presented in the MolPort-000-883-864 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MolPort-000-883-864 DMF.
A MolPort-000-883-864 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MolPort-000-883-864 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-000-883-864 suppliers with CEP (COS) on PharmaCompass.
We have 13 companies offering MolPort-000-883-864
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