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01 1Aspen Pharmacare Holdings

02 3Apotex Inc

03 1Auro Pharma Inc

04 8Aurobindo Pharma Limited

05 1Aurovitas Spain, Sau

06 2Chartwell Pharmaceuticals llc

07 5Cipla

08 1Grupo Chemo

09 1Halewood Laboratories Pvt. Ltd

10 5Hetero Drugs

11 1JAMP PHARMA

12 1Laurus Labs

13 1Lupin Ltd

14 1MINT PHARMACEUTICALS INC

15 2Macleods Pharmaceuticals Limited

16 1Medical Valley

17 1Norvium

18 2Novagen Pharma

19 1STADA Arzneimittel

20 2Sun Pharmaceutical Industries Limited

21 1Tarbis Farma Sl

22 2Teva Pharmaceutical Industries

23 11Viatris

24 22ViiV Healthcare

25 2Zentiva

26 1Zydus Pharmaceuticals

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PharmaCompass

01

Abacavir Sulphate

Brand Name : Aspen Abacavir 300

Dosage Form : TAB

Dosage Strength : 300mg

Packaging : 60X1mg

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

02

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ABACAVIR SULFATE

Brand Name : ABACAVIR SULFATE

Dosage Form : TABLET; ORAL

Dosage Strength : 60MG

Packaging :

Approval Date :

Application Number : 22293

Regulatory Info :

Registration Country : USA

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03

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ABACAVIR SULFATE; LAMIVUDINE

Brand Name : ABACAVIR SULFATE; LAMIVUDINE

Dosage Form : TABLET; ORAL

Dosage Strength : 60MG; 30MG

Packaging :

Approval Date :

Application Number : 22295

Regulatory Info :

Registration Country : USA

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04

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ABACAVIR SULFATE

Brand Name : ABACAVIR SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 300MG BASE

Packaging :

Approval Date : 2012-12-17

Application Number : 77844

Regulatory Info : RX

Registration Country : USA

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05

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ABACAVIR SULFATE

Brand Name : ABACAVIR SULFATE

Dosage Form : SOLUTION;ORAL

Dosage Strength : EQ 20MG BASE/ML

Packaging :

Approval Date : 2018-03-14

Application Number : 77950

Regulatory Info : RX

Registration Country : USA

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06

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ABACAVIR SULFATE; LAMIVUDINE

Brand Name : ABACAVIR SULFATE AND LAMIVUDINE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 600MG BASE;300MG

Packaging :

Approval Date : 2018-11-15

Application Number : 90159

Regulatory Info : RX

Registration Country : USA

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07

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ABACAVIR SULFATE

Brand Name : ABACAVIR SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 300MG BASE

Packaging :

Approval Date : 2016-10-28

Application Number : 91050

Regulatory Info : RX

Registration Country : USA

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09

ABACAVIR SULFATE

Brand Name : ABACAVIR SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 300MG BASE

Packaging :

Approval Date : 2017-11-21

Application Number : 78119

Regulatory Info : RX

Registration Country : USA

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11

ABACAVIR SULFATE; LAMIVUDINE

Brand Name : ABACAVIR SULFATE AND LAMIVUDINE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 600MG BASE;300MG

Packaging :

Approval Date : 2017-03-28

Application Number : 91144

Regulatory Info : RX

Registration Country : USA

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12

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ABACAVIR SULFATE; LAMIVUDINE

Brand Name : ABACAVIR SULFATE AND LAMIVUDINE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 600MG BASE;300MG

Packaging :

Approval Date : 2016-09-29

Application Number : 79246

Regulatory Info : DISCN

Registration Country : USA

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13

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ABACAVIR SULFATE

Brand Name : ABACAVIR SULFATE

Dosage Form : TABLET; ORAL

Dosage Strength : 300MG

Packaging :

Approval Date :

Application Number : 78742

Regulatory Info :

Registration Country : USA

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14

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ABACAVIR SULFATE; LAMIVUDINE; ZIDOVUDINE

Brand Name : ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE

Dosage Form : TABLET; ORAL

Dosage Strength : EQ 300MG BASE; 150MG; 300MG

Packaging :

Approval Date :

Application Number : 90309

Regulatory Info :

Registration Country : USA

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15

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ABACAVIR SULFATE; LAMIVUDINE

Brand Name : ABACAVIR SULFATE; LAMIVUDINE

Dosage Form : TABLET; ORAL

Dosage Strength : 600MG; 300MG

Packaging :

Approval Date :

Application Number : 90519

Regulatory Info :

Registration Country : USA

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16

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ABACAVIR SULFATE

Brand Name : ABACAVIR SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 300MG BASE

Packaging :

Approval Date : 2012-06-18

Application Number : 91294

Regulatory Info : RX

Registration Country : USA

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17

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ABACAVIR SULFATE

Brand Name : ZIAGEN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1998-12-17

Application Number : 20977

Regulatory Info : DISCN

Registration Country : USA

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18

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ABACAVIR SULFATE

Brand Name : ZIAGEN

Dosage Form : SOLUTION;ORAL

Dosage Strength : EQ 20MG BASE/ML

Packaging :

Approval Date : 1998-12-17

Application Number : 20978

Regulatory Info : RX

Registration Country : USA

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19

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ABACAVIR SULFATE; LAMIVUDINE; ZIDOVUDINE

Brand Name : TRIZIVIR

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 300MG BASE;150MG;300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2000-11-14

Application Number : 21205

Regulatory Info : DISCN

Registration Country : USA

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20

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ABACAVIR SULFATE; LAMIVUDINE

Brand Name : EPZICOM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 600MG BASE;300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2004-08-02

Application Number : 21652

Regulatory Info : DISCN

Registration Country : USA

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