Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1Symbiotec Pharmalab
02 1Curia
03 1ACS DOBFAR SPA
04 1Fujifilm Diosynth Biotechnologies
05 1Henan Lihua Pharmaceutical
06 1Merck & Co
07 1NEWCHEM SPA
08 1Pfizer Inc
09 1Quimica Sintetica
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
GDUFA
DMF Review : Complete
Rev. Date : 2016-06-10
Pay. Date : 2016-05-27
DMF Number : 23899
Submission : 2010-06-18
Status :
Type : II
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
GDUFA
DMF Review : Complete
Rev. Date : 2014-02-12
Pay. Date : 2013-09-12
DMF Number : 22624
Submission : 2009-03-13
Status :
Type : II
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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.
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A Sodium prednisolone phosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium prednisolone phosphate, including repackagers and relabelers. The FDA regulates Sodium prednisolone phosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium prednisolone phosphate 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 Sodium prednisolone phosphate supplier is an individual or a company that provides Sodium prednisolone phosphate active pharmaceutical ingredient (API) or Sodium prednisolone phosphate finished formulations upon request. The Sodium prednisolone phosphate suppliers may include Sodium prednisolone phosphate API manufacturers, exporters, distributors and traders.
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A Sodium prednisolone phosphate DMF (Drug Master File) is a document detailing the whole manufacturing process of Sodium prednisolone phosphate active pharmaceutical ingredient (API) in detail. Different forms of Sodium prednisolone phosphate DMFs exist exist since differing nations have different regulations, such as Sodium prednisolone phosphate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sodium prednisolone phosphate DMF submitted to regulatory agencies in the US is known as a USDMF. Sodium prednisolone phosphate USDMF includes data on Sodium prednisolone phosphate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sodium prednisolone phosphate USDMF is kept confidential to protect the manufacturer’s intellectual property.
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