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
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 : R1-CEP 2011-149 - Rev 01
Status : Valid
Issue Date : 2022-02-15
Type : Chemical
Substance Number : 735
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Certificate Number : CEP 2023-025 - Rev 00
Status : Valid
Issue Date : 2025-03-04
Type : Chemical
Substance Number : 735

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Certificate Number : R1-CEP 2016-329 - Rev 00
Status : Valid
Issue Date : 2023-07-13
Type : Chemical
Substance Number : 735

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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 Optival manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Optival, including repackagers and relabelers. The FDA regulates Optival manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Optival 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 Optival manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Optival supplier is an individual or a company that provides Optival active pharmaceutical ingredient (API) or Optival finished formulations upon request. The Optival suppliers may include Optival API manufacturers, exporters, distributors and traders.
click here to find a list of Optival suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Optival CEP of the European Pharmacopoeia monograph is often referred to as a Optival Certificate of Suitability (COS). The purpose of a Optival CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Optival EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Optival to their clients by showing that a Optival CEP has been issued for it. The manufacturer submits a Optival CEP (COS) as part of the market authorization procedure, and it takes on the role of a Optival CEP holder for the record. Additionally, the data presented in the Optival CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Optival DMF.
A Optival CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Optival 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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