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01 2Sanofi

02 5AAIPharma Services Corp.

03 11ANI Pharmaceuticals Inc

04 6Actavis Inc

05 6Alembic Pharmaceuticals Limited

06 6Amneal Pharmaceuticals

07 6Avet Pharmaceuticals

08 6Chartwell Pharmaceuticals llc

09 6Novast Laboratories

10 5Pharmascience Inc.

11 4USL PHARMA

12 6VALIDUS PHARMS

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PharmaCompass

01

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Fi Europe 2024
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : DISCN

Registration Country : USA

DESIPRAMINE HYDROCHLORIDE

Brand Name : PERTOFRANE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 25MG

Packaging :

Approval Date : 1982-01-01

Application Number : 13621

Regulatory Info : DISCN

Registration Country : USA

Sanofi Company Banner

02

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Fi Europe 2024
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : DISCN

Registration Country : USA

DESIPRAMINE HYDROCHLORIDE

Brand Name : PERTOFRANE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1982-01-01

Application Number : 13621

Regulatory Info : DISCN

Registration Country : USA

Sanofi Company Banner

03

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1987-06-05

Application Number : 71588

Regulatory Info : RX

Registration Country : USA

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04

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG

Packaging :

Approval Date : 1987-06-05

Application Number : 71601

Regulatory Info : RX

Registration Country : USA

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05

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 75MG

Packaging :

Approval Date : 1987-10-05

Application Number : 71602

Regulatory Info : RX

Registration Country : USA

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06

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1987-10-05

Application Number : 71766

Regulatory Info : RX

Registration Country : USA

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07

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 1996-02-09

Application Number : 74430

Regulatory Info : RX

Registration Country : USA

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08

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 150MG

Packaging :

Approval Date : 1996-02-09

Application Number : 74430

Regulatory Info : RX

Registration Country : USA

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09

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1997-05-29

Application Number : 71803

Regulatory Info : DISCN

Registration Country : USA

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10

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG

Packaging :

Approval Date : 1987-12-08

Application Number : 71803

Regulatory Info : DISCN

Registration Country : USA

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11

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1987-12-08

Application Number : 71803

Regulatory Info : DISCN

Registration Country : USA

blank

12

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 75MG

Packaging :

Approval Date : 1987-12-08

Application Number : 71803

Regulatory Info : DISCN

Registration Country : USA

blank

13

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 150MG

Packaging :

Approval Date : 1997-05-29

Application Number : 71803

Regulatory Info : DISCN

Registration Country : USA

blank

14

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1988-06-20

Application Number : 72103

Regulatory Info : RX

Registration Country : USA

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15

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 1988-05-24

Application Number : 72103

Regulatory Info : RX

Registration Country : USA

blank

16

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG

Packaging :

Approval Date : 1988-05-24

Application Number : 72103

Regulatory Info : RX

Registration Country : USA

blank

17

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1988-05-24

Application Number : 72103

Regulatory Info : RX

Registration Country : USA

blank

18

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 75MG

Packaging :

Approval Date : 1988-06-20

Application Number : 72103

Regulatory Info : RX

Registration Country : USA

blank

19

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 150MG

Packaging :

Approval Date : 1988-06-20

Application Number : 72103

Regulatory Info : RX

Registration Country : USA

blank

20

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2017-12-26

Application Number : 204963

Regulatory Info : RX

Registration Country : USA

blank

21

USL PHARMA

United Kingdom
Fi Europe 2024
Not Confirmed
arrow

USL PHARMA

United Kingdom
arrow
Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG

Packaging :

Approval Date : 1987-09-09

Application Number : 71864

Regulatory Info : DISCN

Registration Country : USA

blank

22

USL PHARMA

United Kingdom
Fi Europe 2024
Not Confirmed
arrow

USL PHARMA

United Kingdom
arrow
Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1987-09-09

Application Number : 71865

Regulatory Info : DISCN

Registration Country : USA

blank

23

USL PHARMA

United Kingdom
Fi Europe 2024
Not Confirmed
arrow

USL PHARMA

United Kingdom
arrow
Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 75MG

Packaging :

Approval Date : 1987-09-09

Application Number : 71866

Regulatory Info : DISCN

Registration Country : USA

blank

24

USL PHARMA

United Kingdom
Fi Europe 2024
Not Confirmed
arrow

USL PHARMA

United Kingdom
arrow
Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : DESIPRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1987-09-09

Application Number : 71867

Regulatory Info : DISCN

Registration Country : USA

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25

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : NORPRAMIN

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG

Packaging :

Approval Date : 1982-01-01

Application Number : 14399

Regulatory Info : RX

Registration Country : USA

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26

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : NORPRAMIN

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1982-01-01

Application Number : 14399

Regulatory Info : RX

Registration Country : USA

blank

27

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : NORPRAMIN

Dosage Form : TABLET;ORAL

Dosage Strength : 75MG

Packaging :

Approval Date : 1982-01-01

Application Number : 14399

Regulatory Info : RX

Registration Country : USA

blank

28

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : NORPRAMIN

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 14399

Regulatory Info : RX

Registration Country : USA

blank

29

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : NORPRAMIN

Dosage Form : TABLET;ORAL

Dosage Strength : 150MG

Packaging :

Approval Date : 1982-01-01

Application Number : 14399

Regulatory Info : RX

Registration Country : USA

blank

30

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

DESIPRAMINE HYDROCHLORIDE

Brand Name : NORPRAMIN

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 1982-02-11

Application Number : 14399

Regulatory Info : RX

Registration Country : USA

blank