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01 2STRIDES PHARMA

02 2ALVOGEN

03 2CADILA PHARMS LTD

04 2DR REDDYS LABS LTD

05 2NOVARTIS

06 2RISING

07 2TEVA PHARMS

08 2WATSON LABS

09 2ZYDUS PHARMS

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

RLD : No

TE Code : AB

NATEGLINIDE

Brand Name : NATEGLINIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 60MG

Approval Date : 2009-09-09

Application Number : 77463

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Strides Pharma Science

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

RLD : No

TE Code : AB

NATEGLINIDE

Brand Name : NATEGLINIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 120MG

Approval Date : 2009-09-09

Application Number : 77463

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Strides Pharma Science

03

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
Not Confirmed

NATEGLINIDE

Brand Name : NATEGLINIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 60MG

Approval Date : 2011-03-30

Application Number : 77462

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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04

2024 ACI Convention
Not Confirmed
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arrow
2024 ACI Convention
Not Confirmed

NATEGLINIDE

Brand Name : NATEGLINIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 120MG

Approval Date : 2011-03-30

Application Number : 77462

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

blank

05

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
Not Confirmed

NATEGLINIDE

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Dosage Strength : 60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2000-12-22

Application Number : 21204

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

2024 ACI Convention
Not Confirmed
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arrow
2024 ACI Convention
Not Confirmed

NATEGLINIDE

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**

Approval Date : 2000-12-22

Application Number : 21204

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

07

2024 ACI Convention
Not Confirmed
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arrow
2024 ACI Convention
Not Confirmed

NATEGLINIDE

Brand Name : NATEGLINIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 60MG

Approval Date : 2009-09-09

Application Number : 77467

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

08

2024 ACI Convention
Not Confirmed
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arrow
2024 ACI Convention
Not Confirmed

NATEGLINIDE

Brand Name : NATEGLINIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 120MG

Approval Date : 2009-09-09

Application Number : 77467

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

09

DR REDDYS LABS LTD

2024 ACI Convention
Not Confirmed
arrow

DR REDDYS LABS LTD

arrow
2024 ACI Convention
Not Confirmed

NATEGLINIDE

Brand Name : NATEGLINIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 60MG

Approval Date : 2009-09-09

Application Number : 77461

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

blank

10

DR REDDYS LABS LTD

2024 ACI Convention
Not Confirmed
arrow

DR REDDYS LABS LTD

arrow
2024 ACI Convention
Not Confirmed

NATEGLINIDE

Brand Name : NATEGLINIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 120MG

Approval Date : 2009-09-09

Application Number : 77461

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

blank