Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
01 1Pfizer CentreOne
02 1EUROAPI
03 2ACS DOBFAR SPA
04 1Compañía Casco
05 1Curia
06 1Fujifilm Diosynth Biotechnologies
07 1Henan Lihua Pharmaceutical
08 1Mahima Life Sciences
09 1Merck & Co
10 1SIMS Srl
11 1Symbiotica
12 2Tianjin Tianfa Pharmaceutical Import & Export
13 1Xi'an Guokang Ruijin Pharmaceutical
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
GDUFA
DMF Review : Complete
Rev. Date : 2022-03-04
Pay. Date : 2022-02-28
DMF Number : 6525
Submission : 1986-08-11
Status :
Type : II
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
GDUFA
DMF Review : Complete
Rev. Date : 2013-01-28
Pay. Date : 2013-01-16
DMF Number : 3963
Submission : 1980-10-10
Status :
Type : II
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PharmaCompass offers a list of Dexamethasone 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 Dexamethasone Sodium Phosphate manufacturer or Dexamethasone Sodium Phosphate supplier for your needs.
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A Hexadrol Injectable manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hexadrol Injectable, including repackagers and relabelers. The FDA regulates Hexadrol Injectable manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hexadrol Injectable 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 Hexadrol Injectable supplier is an individual or a company that provides Hexadrol Injectable active pharmaceutical ingredient (API) or Hexadrol Injectable finished formulations upon request. The Hexadrol Injectable suppliers may include Hexadrol Injectable API manufacturers, exporters, distributors and traders.
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A Hexadrol Injectable DMF (Drug Master File) is a document detailing the whole manufacturing process of Hexadrol Injectable active pharmaceutical ingredient (API) in detail. Different forms of Hexadrol Injectable DMFs exist exist since differing nations have different regulations, such as Hexadrol Injectable USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Hexadrol Injectable DMF submitted to regulatory agencies in the US is known as a USDMF. Hexadrol Injectable USDMF includes data on Hexadrol Injectable's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Hexadrol Injectable USDMF is kept confidential to protect the manufacturer’s intellectual property.
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