Veranova: A CDMO that manages complexity with confidence.
01 3Veranova
02 3Noramco
03 1Chattem Chemicals, Inc
04 3Mallinckrodt Pharmaceuticals
05 3Siegfried AG
Veranova: A CDMO that manages complexity with confidence.
GDUFA
DMF Review : Complete
Rev. Date : 2014-06-21
Pay. Date : 2014-06-13
DMF Number : 18472
Submission : 2005-06-30
Status :
Type : II
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
GDUFA
DMF Review : Complete
Rev. Date : 2013-04-16
Pay. Date : 2013-04-05
DMF Number : 16399
Submission : 2003-02-03
Status :
Type : II
Veranova: A CDMO that manages complexity with confidence.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34028
Submission : 2019-10-14
Status :
Type : II
Veranova: A CDMO that manages complexity with confidence.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32506
Submission : 2018-03-16
Status :
Type : II
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
GDUFA
DMF Review : Complete
Rev. Date : 2012-12-27
Pay. Date : 2012-11-23
DMF Number : 20975
Submission : 2007-10-26
Status :
Type : II
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
GDUFA
DMF Review : Complete
Rev. Date : 2013-02-15
Pay. Date : 2012-11-23
DMF Number : 21353
Submission : 2008-02-21
Status :
Type : II
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PharmaCompass offers a list of Oxycodone Hydrochloride 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 Oxycodone Hydrochloride manufacturer or Oxycodone Hydrochloride supplier for your needs.
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A Eukodal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eukodal, including repackagers and relabelers. The FDA regulates Eukodal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eukodal 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 Eukodal supplier is an individual or a company that provides Eukodal active pharmaceutical ingredient (API) or Eukodal finished formulations upon request. The Eukodal suppliers may include Eukodal API manufacturers, exporters, distributors and traders.
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A Eukodal DMF (Drug Master File) is a document detailing the whole manufacturing process of Eukodal active pharmaceutical ingredient (API) in detail. Different forms of Eukodal DMFs exist exist since differing nations have different regulations, such as Eukodal USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Eukodal DMF submitted to regulatory agencies in the US is known as a USDMF. Eukodal USDMF includes data on Eukodal's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Eukodal USDMF is kept confidential to protect the manufacturer’s intellectual property.
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