Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
01 4Strides Pharma Science
02 2Actavis Inc
03 2Alvogen
04 3Biofarma Pharmaceutical Industry and Commerce Inc
05 2Cadila Pharmaceuticals
06 3Humanis
07 2Myungmoon Pharm. Co., LTD.
08 2Nobel Ilac Sanayii Ve Ticaret A.S.
09 2Novartis Pharmaceuticals Corporation
10 1Novartis South Africa (Pty) Ltd
11 2Rising Pharmaceuticals Inc
12 2Teva Pharmaceutical Industries
13 4Unichem Laboratories Limited
14 1Wanbang Biopharmaceuticals
15 6World Medicine
16 2XYZ Pharma
17 1Yangtze River Pharmaceutical Group
18 2Zydus Lifesciences
19 2Zydus Pharmaceuticals
01 3FC Tablet
02 1FCT
03 6FILM COATED TABLET
04 5Film Coated Tablet
05 2TABLET
06 18TABLET;ORAL
07 10Tablet
01 6DISCN
02 10Generic
03 2Generic B.E study
04 1Originator
05 12RX
06 14Blank
01 3Dianide
02 2Glinade
03 16NATEGLINIDE
04 2Natalix
05 3REAGLID
06 2STARLIX
07 1Starlix
08 3Teglix
09 13Blank
01 2China
02 8India
03 1South Africa
04 2South Korea
05 14Turkey
06 18USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NATEGLINIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 60MG
Packaging :
Approval Date : 2009-09-09
Application Number : 77463
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NATEGLINIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 120MG
Packaging :
Approval Date : 2009-09-09
Application Number : 77463
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 60MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 120MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : RX
Registration Country : USA
Brand Name : NATEGLINIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 60MG
Packaging :
Approval Date : 2011-03-30
Application Number : 77462
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NATEGLINIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 120MG
Packaging :
Approval Date : 2011-03-30
Application Number : 77462
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NATEGLINIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 60MG
Packaging :
Approval Date : 2015-12-11
Application Number : 205055
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NATEGLINIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 120MG
Packaging :
Approval Date : 2015-12-11
Application Number : 205055
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Generic
Registration Country : Turkey
Brand Name : Dianide
Dosage Form : Film Coated Tablet
Dosage Strength : 60MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Turkey
Regulatory Info : Generic
Registration Country : Turkey
Brand Name : Dianide
Dosage Form : Film Coated Tablet
Dosage Strength : 120MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Turkey
Regulatory Info : Generic
Registration Country : Turkey
Brand Name : Dianide
Dosage Form : Film Coated Tablet
Dosage Strength : 180MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Turkey
Regulatory Info : Generic B.E study
Registration Country : South Korea
Brand Name : Glinade
Dosage Form : TABLET
Dosage Strength : 90MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic B.E study
Registration Country : South Korea
Regulatory Info : Generic B.E study
Registration Country : South Korea
Brand Name : Glinade
Dosage Form : TABLET
Dosage Strength : 120MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic B.E study
Registration Country : South Korea
Regulatory Info :
Registration Country : Turkey
Brand Name : Natalix
Dosage Form : Film Coated Tablet
Dosage Strength : 120MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Turkey
Regulatory Info :
Registration Country : Turkey
Brand Name : Natalix
Dosage Form : Film Coated Tablet
Dosage Strength : 180MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Turkey
Regulatory Info : DISCN
Registration Country : USA
Brand Name : STARLIX
Dosage Form : TABLET;ORAL
Dosage Strength : 60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2000-12-22
Application Number : 21204
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : STARLIX
Dosage Form : TABLET;ORAL
Dosage Strength : 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2000-12-22
Application Number : 21204
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NATEGLINIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 60MG
Packaging :
Approval Date : 2018-06-18
Application Number : 205544
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NATEGLINIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 120MG
Packaging :
Approval Date : 2018-06-18
Application Number : 205544
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NATEGLINIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 60MG
Packaging :
Approval Date : 2009-09-09
Application Number : 77467
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NATEGLINIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 120MG
Packaging :
Approval Date : 2009-09-09
Application Number : 77467
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Generic
Registration Country : Turkey
Brand Name :
Dosage Form : FILM COATED TABLET
Dosage Strength : 60MG
Packaging : 84 Tablets
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Turkey
Regulatory Info : Generic
Registration Country : Turkey
Brand Name :
Dosage Form : FILM COATED TABLET
Dosage Strength : 120MG
Packaging : 84 Tablets
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Turkey
Regulatory Info : Generic
Registration Country : Turkey
Brand Name :
Dosage Form : FILM COATED TABLET
Dosage Strength : 180MG
Packaging : 84 Tablets
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Turkey
Regulatory Info : RX
Registration Country : USA
Brand Name : NATEGLINIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 60MG
Packaging :
Approval Date : 2009-09-09
Application Number : 77461
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NATEGLINIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 120MG
Packaging :
Approval Date : 2009-09-09
Application Number : 77461
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NATEGLINIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 60MG
Packaging :
Approval Date : 2019-04-19
Application Number : 206432
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NATEGLINIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 120MG
Packaging :
Approval Date : 2019-04-19
Application Number : 206432
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NATEGLINIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 60MG
Packaging :
Approval Date : 2016-07-06
Application Number : 205248
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NATEGLINIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 120MG
Packaging :
Approval Date : 2016-07-06
Application Number : 205248
Regulatory Info : RX
Registration Country : USA
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