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01 4BRECKENRIDGE

02 3ACTAVIS ELIZABETH

03 4AJANTA PHARMA LTD

04 3ALEMBIC

05 3ALKEM LABS LTD

06 3APOTEX

07 3AUROBINDO PHARMA LTD

08 3CSPC OUYI

09 3ENDO OPERATIONS

10 3HETERO LABS LTD III

11 3IMPAX LABS INC

12 3INVENTIA

13 12LILLY

14 4LUPIN LTD

15 3MACLEODS PHARMS LTD

16 3MARKSANS PHARMA

17 3PRINSTON INC

18 3QINGDAO BAHEAL PHARM

19 3SANDOZ

20 7SUN PHARM

21 3SUNSHINE

22 3TEVA PHARMS USA

23 3TORRENT

24 3WOCKHARDT

25 3YAOPHARMA CO LTD

26 4ZYDUS HLTHCARE

27 3ZYDUS PHARMS

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PharmaCompass

01

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Pharmtech & Ingredients
Not Confirmed

DULOXETINE HYDROCHLORIDE

Brand Name : DULOXETINE HYDROCHLORIDE

Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL

Dosage Strength : EQ 20MG BASE

Approval Date : 2014-06-11

Application Number : 203088

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Breckenridge Pharmaceutical

02

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Pharmtech & Ingredients
Not Confirmed

DULOXETINE HYDROCHLORIDE

Brand Name : DULOXETINE HYDROCHLORIDE

Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL

Dosage Strength : EQ 30MG BASE

Approval Date : 2014-06-11

Application Number : 203088

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Breckenridge Pharmaceutical

03

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Pharmtech & Ingredients
Not Confirmed

DULOXETINE HYDROCHLORIDE

Brand Name : DULOXETINE HYDROCHLORIDE

Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL

Dosage Strength : EQ 60MG BASE

Approval Date : 2014-06-11

Application Number : 203088

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Breckenridge Pharmaceutical

04

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Pharmtech & Ingredients
Not Confirmed

DULOXETINE HYDROCHLORIDE

Brand Name : DULOXETINE HYDROCHLORIDE

Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL

Dosage Strength : EQ 40MG BASE

Approval Date : 2018-05-18

Application Number : 203088

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Breckenridge Pharmaceutical

05

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

DULOXETINE HYDROCHLORIDE

Brand Name : CYMBALTA

Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL

Dosage Strength : EQ 20MG BASE

Approval Date : 2004-08-03

Application Number : 21427

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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06

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

DULOXETINE HYDROCHLORIDE

Brand Name : CYMBALTA

Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL

Dosage Strength : EQ 30MG BASE

Approval Date : 2004-08-03

Application Number : 21427

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

blank

07

Pharmtech & Ingredients
Not Confirmed
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arrow
Pharmtech & Ingredients
Not Confirmed

DULOXETINE HYDROCHLORIDE

Brand Name : CYMBALTA

Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL

Dosage Strength : EQ 60MG BASE

Approval Date : 2004-08-03

Application Number : 21427

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

blank

08

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

DULOXETINE HYDROCHLORIDE

Brand Name : CYMBALTA

Dosage Form : CAPSULE, DELAYED REL PELLETS; ORAL

Dosage Strength : EQ 20MG BASE

Approval Date :

Application Number : 21733

RX/OTC/DISCN :

RLD :

TE Code :

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09

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

DULOXETINE HYDROCHLORIDE

Brand Name : CYMBALTA

Dosage Form : CAPSULE, DELAYED REL PELLETS; ORAL

Dosage Strength : EQ 30MG BASE

Approval Date :

Application Number : 21733

RX/OTC/DISCN :

RLD :

TE Code :

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10

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

DULOXETINE HYDROCHLORIDE

Brand Name : CYMBALTA

Dosage Form : CAPSULE, DELAYED REL PELLETS; ORAL

Dosage Strength : EQ 60MG BASE

Approval Date :

Application Number : 21733

RX/OTC/DISCN :

RLD :

TE Code :

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