01 1AVIK PHARMACEUTICAL LIMITED Vapi IN
02 2HENAN LIHUA PHARMACEUTICAL CO., LTD. Anyang CN
03 2SYMBIOTEC PHARMALAB LIMITED Indore IN
01 3Prednisolone sodium phosphate
02 1Prednisolone sodium phosphate, Process 2
03 1Prednisolone sodium phosphate, Process C
01 2China
02 1India
03 2Blank
01 5Valid
Certificate Number : CEP 2023-025 - Rev 00
Status : Valid
Issue Date : 2025-03-04
Type : Chemical
Substance Number : 735
Certificate Number : CEP 2016-329 - Rev 01
Status : Valid
Issue Date : 2026-04-29
Type : Chemical
Substance Number : 735
Prednisolone Sodium Phosphate, Process C
Certificate Number : CEP 2023-402 - Rev 00
Status : Valid
Issue Date : 2024-04-11
Type : Chemical
Substance Number : 735
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Prednisolone Sodium Phosphate, Process 2
Certificate Number : CEP 2016-205 - Rev 02
Status : Valid
Issue Date : 2026-04-01
Type : Chemical
Substance Number : 735
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Certificate Number : CEP 2011-149 - Rev 02
Status : Valid
Issue Date : 2026-04-02
Type : Chemical
Substance Number : 735
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PharmaCompass offers a list of Prednisolone Sodium Phosphate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Prednisolone Sodium Phosphate manufacturer or Prednisolone Sodium Phosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Prednisolone Sodium Phosphate manufacturer or Prednisolone Sodium Phosphate supplier.
A Prozorin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prozorin, including repackagers and relabelers. The FDA regulates Prozorin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prozorin 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 Prozorin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Prozorin supplier is an individual or a company that provides Prozorin active pharmaceutical ingredient (API) or Prozorin finished formulations upon request. The Prozorin suppliers may include Prozorin API manufacturers, exporters, distributors and traders.
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A Prozorin CEP of the European Pharmacopoeia monograph is often referred to as a Prozorin Certificate of Suitability (COS). The purpose of a Prozorin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Prozorin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Prozorin to their clients by showing that a Prozorin CEP has been issued for it. The manufacturer submits a Prozorin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Prozorin CEP holder for the record. Additionally, the data presented in the Prozorin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Prozorin DMF.
A Prozorin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Prozorin 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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