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// Press Release FDA
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15933
Submission : 2002-03-18
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18989
Submission : 2005-11-28
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15933
Submission : 2002-03-18
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18989
Submission : 2005-11-28
Status : Inactive
Type : II
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : HYDROCODONE BITARTRATE A...
Dosage Strength : 500MG;5MG
Approval Date : 1988-04-21
Application Number : 89696
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : CAPSULE; ORAL
Proprietary Name : ALLAY
Dosage Strength : 500MG;5MG
Approval Date : 1989-01-13
Application Number : 89907
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Dosage Form : TABLET; ORAL
Proprietary Name : PROPOXYPHENE NAPSYLATE A...
Dosage Strength : 650MG;100MG
Approval Date : 1985-08-02
Application Number : 70146
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : ACYCLOVIR
Dosage Strength : 200MG
Approval Date : 1997-04-22
Application Number : 74674
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ACYCLOVIR
Dosage Strength : 400MG
Approval Date : 1997-04-22
Application Number : 74836
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ACYCLOVIR
Dosage Strength : 800MG
Approval Date : 1997-04-22
Application Number : 74836
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : AEROSOL, METERED; INHALATION
Proprietary Name : ALBUTEROL
Dosage Strength : 0.09MG/INH
Approval Date : 1995-12-28
Application Number : 73272
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ALPRAZOLAM
Dosage Strength : 0.25MG
Approval Date : 1994-07-29
Application Number : 74294
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ALPRAZOLAM
Dosage Strength : 0.5MG
Approval Date : 1994-07-29
Application Number : 74294
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ALPRAZOLAM
Dosage Strength : 1MG
Approval Date : 1994-07-29
Application Number : 74294
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Inspections and registrations
District Decision : No Action Indicated
Inspection End Date : 2010-01-26
City : Doral
State : FL
Country/Area : US
Zip : 33178-2404
District : FLA
Center : CDER
Project Area : Drug Quality Assurance
District Decision : No Action Indicated
Inspection End Date : 2010-01-26
District Decision : No Action Indicated
Inspection End Date : 2013-06-06
City : Doral
State : FL
Country/Area : US
Zip : 33178-2404
District : FLA
Center : CDER
Project Area : Drug Quality Assurance
District Decision : No Action Indicated
Inspection End Date : 2013-06-06
District Decision : Voluntary Action Indicated
Inspection End Date : 2009-04-22
City : Runcorn
State :
Country/Area : GB
Zip :
District : ORA
Center : CDER
Project Area : Drug Quality Assurance
District Decision : Voluntary Action Indicated
Inspection End Date : 2009-04-22
District Decision : Voluntary Action Indicated
Inspection End Date : 2010-11-19
City : Runcorn
State :
Country/Area : GB
Zip :
District : ORA
Center : CDER
Project Area : Drug Quality Assurance
District Decision : Voluntary Action Indicated
Inspection End Date : 2010-11-19
District Decision : Voluntary Action Indicated
Inspection End Date : 2012-11-06
City : Runcorn
State :
Country/Area : GB
Zip :
District : ORA
Center : CDER
Project Area : Drug Quality Assurance
District Decision : Voluntary Action Indicated
Inspection End Date : 2012-11-06
District Decision : Voluntary Action Indicated
Inspection End Date : 2014-11-11
City : Runcorn
State :
Country/Area : GB
Zip :
District : ORA
Center : CDER
Project Area : Drug Quality Assurance
District Decision : Voluntary Action Indicated
Inspection End Date : 2014-11-11
API Manufacturer :
FDF Manufacturer : FDF MANUFACTURE
Facility Name : Norton Healthcare Limited T/A ...
Business Address : Aston Lane North, Whitehouse...
FEI Number : 3003925187
Country : U.S.A
Paid in : 2019
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IVAX Pharmaceuticals Inc is a supplier offers 2 products (APIs, Excipients or Intermediates).
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