IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
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01 2IOL CHEMICALS AND PHARMACEUTICALS LTD Ludhiana IN
02 1ARCH PHARMALABS LIMITED Mumbai IN
03 1BASF SE Ludwigshafen DE
04 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
05 1Doctors Organic Chemicals Ltd Tanuku (Po) IN
06 1HUBEI BIOCAUSE HEILEN PHARMACEUTICAL CO., LTD. Jingmen City CN
07 1PIRAMAL PHARMA LIMITED Digwal Village IN
08 1SHANDONG XINHUA PHARMACEUTICAL CO., LTD. Zibo CN
09 1SI GROUP, INC. The Woodlands US
10 2SMS PHARMACEUTICALS LIMITED Hyderabad IN
11 1SOLARA ACTIVE PHARMA SCIENCES LIMITED Chennai IN
12 1ZHEJIANG NHU COMPANY LTD. Shaoxing City CN
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01 10Ibuprofen
02 1Ibuprofen, Hexanes route
03 1Ibuprofen, IPA route
04 1Ibuprofen, Process II
05 1Ibuprofen, “S250”; “S380”; “S500”; “SN”; “SHD”
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01 3China
02 1Germany
03 8India
04 2U.S.A
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01 1Expired
02 12Valid
03 1Withdrawn by Holder
Certificate Number : R1-CEP 2008-316 - Rev 05
Status : Valid
Issue Date : 2022-07-27
Type : Chemical
Substance Number : 721
Certificate Number : R0-CEP 2021-506 - Rev 01
Status : Valid
Issue Date : 2023-01-26
Type : Chemical
Substance Number : 721
Certificate Number : R1-CEP 2000-114 - Rev 03
Status : Valid
Issue Date : 2014-04-15
Type : Chemical
Substance Number : 721
Certificate Number : R1-CEP 2000-087 - Rev 03
Status : Valid
Issue Date : 2018-12-07
Type : Chemical
Substance Number : 721
Certificate Number : R1-CEP 1998-012 - Rev 10
Status : Valid
Issue Date : 2022-01-07
Type : Chemical
Substance Number : 721
Certificate Number : R1-CEP 1996-058 - Rev 06
Status : Valid
Issue Date : 2022-08-22
Type : Chemical
Substance Number : 721
Certificate Number : CEP 2020-414 - Rev 01
Status : Valid
Issue Date : 2024-03-25
Type : Chemical
Substance Number : 721
Certificate Number : R0-CEP 2021-056 - Rev 00
Status : Valid
Issue Date : 2022-07-21
Type : Chemical
Substance Number : 721
Ibuprofen, “S250”; “S380”; “S500”; ...
Certificate Number : R1-CEP 1996-061 - Rev 15
Status : Valid
Issue Date : 2022-10-28
Type : Chemical
Substance Number : 721
Certificate Number : CEP 2022-354 - Rev 00
Status : Valid
Issue Date : 2024-02-07
Type : Chemical
Substance Number : 721
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PharmaCompass offers a list of Ibuprofen 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 Ibuprofen manufacturer or Ibuprofen supplier for your needs.
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PharmaCompass also assists you with knowing the Ibuprofen API Price utilized in the formulation of products. Ibuprofen API Price is not always fixed or binding as the Ibuprofen Price is obtained through a variety of data sources. The Ibuprofen Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A C13H18O2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C13H18O2, including repackagers and relabelers. The FDA regulates C13H18O2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C13H18O2 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 C13H18O2 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A C13H18O2 supplier is an individual or a company that provides C13H18O2 active pharmaceutical ingredient (API) or C13H18O2 finished formulations upon request. The C13H18O2 suppliers may include C13H18O2 API manufacturers, exporters, distributors and traders.
click here to find a list of C13H18O2 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A C13H18O2 CEP of the European Pharmacopoeia monograph is often referred to as a C13H18O2 Certificate of Suitability (COS). The purpose of a C13H18O2 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of C13H18O2 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of C13H18O2 to their clients by showing that a C13H18O2 CEP has been issued for it. The manufacturer submits a C13H18O2 CEP (COS) as part of the market authorization procedure, and it takes on the role of a C13H18O2 CEP holder for the record. Additionally, the data presented in the C13H18O2 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the C13H18O2 DMF.
A C13H18O2 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. C13H18O2 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 C13H18O2 suppliers with CEP (COS) on PharmaCompass.
We have 11 companies offering C13H18O2
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