Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
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01 2SYMBIOTEC PHARMALAB PRIVATE LIMITED Indore IN
02 1AVIK PHARMACEUTICAL LIMITED Vapi IN
03 2HENAN LIHUA PHARMACEUTICAL CO., LTD. Anyang CN
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01 3Prednisolone sodium phosphate
02 1Prednisolone sodium phosphate, Process 2
03 1Prednisolone sodium phosphate, Process C
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01 2China
02 3India
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01 5Valid
Certificate Number : R1-CEP 2011-149 - Rev 01
Status : Valid
Issue Date : 2022-02-15
Type : Chemical
Substance Number : 735
Prednisolone Sodium Phosphate, Process 2
Certificate Number : R1-CEP 2016-205 - Rev 01
Status : Valid
Issue Date : 2023-06-12
Type : Chemical
Substance Number : 735
Certificate Number : CEP 2023-025 - Rev 00
Status : Valid
Issue Date : 2025-03-04
Type : Chemical
Substance Number : 735
Certificate Number : R1-CEP 2016-329 - Rev 00
Status : Valid
Issue Date : 2023-07-13
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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PharmaCompass offers a list of Prednisolone Sodium Phosphate 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 Prednisolone Sodium Phosphate manufacturer or Prednisolone Sodium Phosphate supplier for your needs.
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PharmaCompass also assists you with knowing the Prednisolone Sodium Phosphate API Price utilized in the formulation of products. Prednisolone Sodium Phosphate API Price is not always fixed or binding as the Prednisolone Sodium Phosphate Price is obtained through a variety of data sources. The Prednisolone Sodium Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vasocidin Solution manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vasocidin Solution, including repackagers and relabelers. The FDA regulates Vasocidin Solution manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vasocidin Solution 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 Vasocidin Solution supplier is an individual or a company that provides Vasocidin Solution active pharmaceutical ingredient (API) or Vasocidin Solution finished formulations upon request. The Vasocidin Solution suppliers may include Vasocidin Solution API manufacturers, exporters, distributors and traders.
click here to find a list of Vasocidin Solution suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vasocidin Solution CEP of the European Pharmacopoeia monograph is often referred to as a Vasocidin Solution Certificate of Suitability (COS). The purpose of a Vasocidin Solution CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Vasocidin Solution EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Vasocidin Solution to their clients by showing that a Vasocidin Solution CEP has been issued for it. The manufacturer submits a Vasocidin Solution CEP (COS) as part of the market authorization procedure, and it takes on the role of a Vasocidin Solution CEP holder for the record. Additionally, the data presented in the Vasocidin Solution CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Vasocidin Solution DMF.
A Vasocidin Solution CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Vasocidin Solution 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 Vasocidin Solution suppliers with CEP (COS) on PharmaCompass.
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