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01 4Dr. Reddy's Laboratories

02 2Strides Pharma Science

03 2AAIPharma Services Corp.

04 4ANI Pharmaceuticals Inc

05 2Arrow Pharmaceuticals

06 4Aurobindo Pharma Limited

07 2Biowise Pharmaceuticals, Sl

08 1Brilliant LifeSciences

09 2Eli Lilly

10 11H. Lundbeck AS

11 1Lucent Biotech Ltd

12 2Macleods Pharmaceuticals Limited

13 5Mallinckrodt Pharmaceuticals

14 2Medreich

15 1PHARM ASSOC

16 2Pharmascience Inc.

17 3Pinewood Healthcare

18 2Pluviaendo

19 4Pulse Pharmaceuticals

20 1RELIANCE FORMULATION PVT. LTD

21 2RIVOPHARM SA

22 1Rekah Pharmaceutical

23 7Ria Generics

24 4Rising Pharmaceuticals Inc

25 1Rubicon Research

26 1Sun Pharmaceutical Industries Limited

27 5Taro Pharmaceutical Industries

28 9Teva Pharmaceutical Industries

29 4Zydus Lifesciences

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : RX

Registration Country : USA

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : NORTRIPTYLINE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 75MG BASE

Packaging :

Approval Date : 1992-03-30

Application Number : 73556

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

Regulatory Info :

Registration Country : India

Nortriptyline

Brand Name : Nortriptyline

Dosage Form : Tablet

Dosage Strength : 10MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : RX

Registration Country : USA

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : NORTRIPTYLINE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 1992-03-30

Application Number : 73556

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : RX

Registration Country : USA

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : NORTRIPTYLINE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 25MG BASE

Packaging :

Approval Date : 1992-03-30

Application Number : 73556

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : RX

Registration Country : USA

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : NORTRIPTYLINE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 50MG BASE

Packaging :

Approval Date : 1992-03-30

Application Number : 73556

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

Regulatory Info :

Registration Country : India

Nortriptyline

Brand Name : Nortriptyline

Dosage Form : Tablet

Dosage Strength : 20MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

07

ISPOR Europe 2025
Not Confirmed
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ISPOR Europe 2025
Not Confirmed

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : NORTRIPTYLINE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 1992-12-31

Application Number : 74054

Regulatory Info : DISCN

Registration Country : USA

blank

08

ISPOR Europe 2025
Not Confirmed
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ISPOR Europe 2025
Not Confirmed

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : NORTRIPTYLINE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 25MG BASE

Packaging :

Approval Date : 1992-12-31

Application Number : 74054

Regulatory Info : DISCN

Registration Country : USA

blank

09

ISPOR Europe 2025
Not Confirmed
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ISPOR Europe 2025
Not Confirmed

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : AVENTYL HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 14684

Regulatory Info : DISCN

Registration Country : USA

blank

10

ISPOR Europe 2025
Not Confirmed
arrow
arrow
ISPOR Europe 2025
Not Confirmed

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : AVENTYL HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 25MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 14684

Regulatory Info : DISCN

Registration Country : USA

blank

11

ISPOR Europe 2025
Not Confirmed
arrow
arrow
ISPOR Europe 2025
Not Confirmed

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : PAMELOR

Dosage Form : SOLUTION;ORAL

Dosage Strength : EQ 10MG BASE/5ML

Packaging :

Approval Date : 1982-01-01

Application Number : 18012

Regulatory Info : DISCN

Registration Country : USA

blank

12

ISPOR Europe 2025
Not Confirmed
arrow
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ISPOR Europe 2025
Not Confirmed

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : PAMELOR

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 18013

Regulatory Info : DISCN

Registration Country : USA

blank

13

ISPOR Europe 2025
Not Confirmed
arrow
arrow
ISPOR Europe 2025
Not Confirmed

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : PAMELOR

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 25MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 18013

Regulatory Info : DISCN

Registration Country : USA

blank

14

ISPOR Europe 2025
Not Confirmed
arrow
arrow
ISPOR Europe 2025
Not Confirmed

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : PAMELOR

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 75MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 18013

Regulatory Info : DISCN

Registration Country : USA

blank

15

ISPOR Europe 2025
Not Confirmed
arrow
arrow
ISPOR Europe 2025
Not Confirmed

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : PAMELOR

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 50MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 18013

Regulatory Info : DISCN

Registration Country : USA

blank

16

ISPOR Europe 2025
Not Confirmed
arrow
arrow
ISPOR Europe 2025
Not Confirmed

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : AVENTYL

Dosage Form : SOLUTION;ORAL

Dosage Strength : EQ 10MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 14685

Regulatory Info : DISCN

Registration Country : USA

blank

17

ISPOR Europe 2025
Not Confirmed
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ISPOR Europe 2025
Not Confirmed

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : NORTRIPTYLINE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 1996-04-11

Application Number : 73667

Regulatory Info : DISCN

Registration Country : USA

blank

18

ISPOR Europe 2025
Not Confirmed
arrow
arrow
ISPOR Europe 2025
Not Confirmed

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : NORTRIPTYLINE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 25MG BASE

Packaging :

Approval Date : 1996-04-11

Application Number : 73667

Regulatory Info : DISCN

Registration Country : USA

blank

19

ISPOR Europe 2025
Not Confirmed
arrow
arrow
ISPOR Europe 2025
Not Confirmed

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : NORTRIPTYLINE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 50MG BASE

Packaging :

Approval Date : 1996-04-11

Application Number : 73667

Regulatory Info : DISCN

Registration Country : USA

blank

20

ISPOR Europe 2025
Not Confirmed
arrow
arrow
ISPOR Europe 2025
Not Confirmed

NORTRIPTYLINE HYDROCHLORIDE

Brand Name : NORTRIPTYLINE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 75MG BASE

Packaging :

Approval Date : 1996-04-11

Application Number : 73667

Regulatory Info : DISCN

Registration Country : USA

blank