Veranova: A CDMO that manages complexity with confidence.
01 3Veranova
02 3Noramco
03 1Chattem Chemicals, Inc
04 3Mallinckrodt Pharmaceuticals
05 3Siegfried AG
01 1OXYCODONE BASE
02 1OXYCODONE BASE - CODE 8180
03 1OXYCODONE HCL
04 3OXYCODONE HYDROCHLORIDE
05 1OXYCODONE HYDROCHLORIDE DRUG SUBSTANCE
06 1OXYCODONE HYDROCHLORIDE PURIFIED RECRYSTALLIZED
07 2OXYCODONE HYDROCHLORIDE USP
08 1OXYCODONE HYDROCHLORIDE USP (D)
09 1OXYCODONE HYDROCHLORIDE, USP
10 1PURIFIED OXYCODONE BASE
01 3Ireland
02 3Switzerland
03 7U.S.A
01 10Active
02 3Inactive
01 7Complete
02 6Blank
GDUFA
DMF Review : Complete
Rev. Date : 2014-06-21
Pay. Date : 2014-06-13
DMF Number : 18472
Submission : 2005-06-30
Status : Active
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 : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32506
Submission : 2018-03-16
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34028
Submission : 2019-10-14
Status : Active
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 : Active
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 : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-04-09
Pay. Date : 2012-11-16
DMF Number : 23419
Submission : 2010-06-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-02-05
Pay. Date : 2012-11-27
DMF Number : 6930
Submission : 1987-04-07
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19898
Submission : 2006-10-17
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-02-07
Pay. Date : 2012-12-27
DMF Number : 23520
Submission : 2010-02-04
Status : Active
Type : II
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.
click here to find a list of Eukodal manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
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.
click here to find a list of Eukodal suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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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