LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
01 3LGM Pharma
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21 2Nostrum Laboratories
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24 1Xixia Pharmaceuticals (Pty) Ltd
01 6Antic-calc Tablet, Film Coated
02 3FILM COATED PILL
03 3Nabumetone 1.000Mg 30 Joined' Oral Use
04 1SOLUBLE TABLET
05 2Soluble Antic-Calc tablet
06 3TAB
07 3TABLET
08 28TABLET;ORAL
09 2TABLETS
01 13DISCN
02 6Generic
03 1Generic B.E study
04 1Prescription
05 15RX
06 15Blank
01 2Artaxan
02 1MEBUTON
03 27NABUMETONE
04 1Osmeton
05 2RELAFEN
06 1Relifen 500
07 13Relifex
08 1Relisan
09 1Relitone
10 2Blank
01 1Canada
02 2India
03 3Italy
04 8Norway
05 3South Africa
06 2South Korea
07 4Sweden
08 28USA
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
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