IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
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
IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
Certificate Number : R0-CEP 2021-506 - Rev 01
Status : Valid
Issue Date : 2023-01-26
Type : Chemical
Substance Number : 721
IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
Certificate Number : R1-CEP 2008-316 - Rev 05
Status : Valid
Issue Date : 2022-07-27
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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A IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE, including repackagers and relabelers. The FDA regulates IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE 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 IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE supplier is an individual or a company that provides IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE active pharmaceutical ingredient (API) or IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE finished formulations upon request. The IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE suppliers may include IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE API manufacturers, exporters, distributors and traders.
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A IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE CEP of the European Pharmacopoeia monograph is often referred to as a IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE Certificate of Suitability (COS). The purpose of a IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE to their clients by showing that a IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE CEP has been issued for it. The manufacturer submits a IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE CEP (COS) as part of the market authorization procedure, and it takes on the role of a IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE CEP holder for the record. Additionally, the data presented in the IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE DMF.
A IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE 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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We have 11 companies offering IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE
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