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01 2ANI Pharmaceuticals Inc

02 2Apotex Fermentation Inc.

03 2Aurobindo Pharma Limited

04 2Avet Pharmaceuticals

05 2Chartwell Pharmaceuticals llc

06 3GSK

07 2Hikma Pharmaceuticals

08 1Kern Pharma S.L.

09 2OrBion Pharmaceuticals

10 2Padagis

11 1Sandoz B2B

12 1Sun Pharmaceutical Industries Limited

13 2Teva Pharmaceutical Industries

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PharmaCompass

01

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2010-07-07

Application Number : 78751

Regulatory Info : DISCN

Registration Country : USA

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02

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2.5MG BASE

Packaging :

Approval Date : 2010-07-07

Application Number : 78751

Regulatory Info : DISCN

Registration Country : USA

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03

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2011-04-22

Application Number : 91373

Regulatory Info : DISCN

Registration Country : USA

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04

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2.5MG BASE

Packaging :

Approval Date : 2011-04-22

Application Number : 91373

Regulatory Info : DISCN

Registration Country : USA

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05

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2012-05-31

Application Number : 202431

Regulatory Info : DISCN

Registration Country : USA

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06

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2.5MG BASE

Packaging :

Approval Date : 2012-05-31

Application Number : 202431

Regulatory Info : DISCN

Registration Country : USA

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07

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2011-02-28

Application Number : 200502

Regulatory Info : RX

Registration Country : USA

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08

Fall Technical Meeting
Not Confirmed
arrow
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2.5MG BASE

Packaging :

Approval Date : 2011-02-28

Application Number : 200502

Regulatory Info : RX

Registration Country : USA

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09

Fall Technical Meeting
Not Confirmed
arrow
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2010-07-07

Application Number : 90288

Regulatory Info : DISCN

Registration Country : USA

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10

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2.5MG BASE

Packaging :

Approval Date : 2010-07-07

Application Number : 90288

Regulatory Info : DISCN

Registration Country : USA

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11

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : AMERGE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1998-02-10

Application Number : 20763

Regulatory Info : DISCN

Registration Country : USA

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12

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : AMERGE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1998-02-10

Application Number : 20763

Regulatory Info : DISCN

Registration Country : USA

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13

Fall Technical Meeting
Not Confirmed
arrow
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2010-07-07

Application Number : 90381

Regulatory Info : RX

Registration Country : USA

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14

Fall Technical Meeting
Not Confirmed
arrow
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2.5MG BASE

Packaging :

Approval Date : 2010-07-07

Application Number : 90381

Regulatory Info : RX

Registration Country : USA

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15

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2012-04-30

Application Number : 91441

Regulatory Info : RX

Registration Country : USA

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16

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2.5MG BASE

Packaging :

Approval Date : 2012-04-30

Application Number : 91441

Regulatory Info : RX

Registration Country : USA

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17

Fall Technical Meeting
Not Confirmed
arrow
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2010-07-08

Application Number : 91326

Regulatory Info : RX

Registration Country : USA

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18

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2.5MG BASE

Packaging :

Approval Date : 2010-07-08

Application Number : 91326

Regulatory Info : RX

Registration Country : USA

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19

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN HYDROCHLORIDE

Brand Name : NARATRIPTAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2.5MG BASE

Packaging :

Approval Date : 2011-02-14

Application Number : 91552

Regulatory Info : DISCN

Registration Country : USA

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20

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

NARATRIPTAN (NARATRIPTAN HYDROCHLORIDE)

Brand Name : TEVA-NARATRIPTAN

Dosage Form : TABLET

Dosage Strength : 1MG

Packaging : 8/60/100

Approval Date :

Application Number : 2314290

Regulatory Info : Prescription

Registration Country : Canada

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