LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
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01 6Antic-calc Tablet, Film Coated
02 1Dispersible Tablet
03 11Film Coated Tablet
04 3Nabumetone 1.000Mg 30 Joined' Oral Use
05 2Orodispersible Tablet
06 2Soluble Antic-Calc tablet
07 3TAB
08 3TABLET
09 30TABLET;ORAL
10 2TABLETS
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01 2Approved
02 1Authorized
03 13DISCN
04 11Deregistered
05 6Generic
06 1Generic B.E study
07 1Prescription
08 17RX
09 11Blank
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01 2Artaxan
02 1MEBUTON
03 29NABUMETONE
04 1Nabumeton Bmm Pharma
05 1Osmeton
06 2RELAFEN
07 1Relif
08 1Relifen 500
09 21Relifex
10 1Relisan
11 1Relitone
12 2Blank
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01 1Canada
02 2India
03 3Italy
04 8Norway
05 3South Africa
06 2South Korea
07 1Spain
08 13Sweden
09 30USA
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Regulatory Info : RX
Registration Country : USA
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Packaging :
Approval Date : 2019-08-30
Application Number : 203166
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Relifen 500
Dosage Form : TAB
Dosage Strength : 500mg
Packaging : 60X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Regulatory Info : RX
Registration Country : USA
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 750MG
Packaging :
Approval Date : 2019-08-30
Application Number : 203166
Regulatory Info : RX
Registration Country : USA
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Regulatory Info : RX
Registration Country : USA
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 1GM
Packaging :
Approval Date : 2019-08-30
Application Number : 203166
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Relitone
Dosage Form : TAB
Dosage Strength : 500mg
Packaging : 60X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : RX
Registration Country : USA
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Packaging :
Approval Date : 2002-02-25
Application Number : 75280
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 750MG
Packaging :
Approval Date : 2002-02-25
Application Number : 75280
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Packaging :
Approval Date : 2003-01-24
Application Number : 76009
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 750MG
Packaging :
Approval Date : 2003-01-24
Application Number : 76009
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 750MG
Packaging :
Approval Date : 2000-06-06
Application Number : 75179
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Packaging :
Approval Date : 2002-02-25
Application Number : 75590
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 750MG
Packaging :
Approval Date : 2002-02-25
Application Number : 75590
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : RELAFEN
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1991-12-24
Application Number : 19583
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : RELAFEN
Dosage Form : TABLET;ORAL
Dosage Strength : 750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1991-12-24
Application Number : 19583
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Packaging :
Approval Date : 2000-05-26
Application Number : 75189
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 750MG
Packaging :
Approval Date : 2001-09-24
Application Number : 75189
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Packaging :
Approval Date : 2008-03-07
Application Number : 78671
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 750MG
Packaging :
Approval Date : 2008-03-07
Application Number : 78671
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Packaging :
Approval Date : 2008-09-24
Application Number : 78420
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 750MG
Packaging :
Approval Date : 2008-09-24
Application Number : 78420
Regulatory Info : RX
Registration Country : USA