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01 1STRIDES ACROLAB

02 2STRIDES ARCOLAB LTD

03 1AM REGENT

04 2AUROBINDO

05 1AUROBINDO PHARMA

06 3AUROBINDO PHARMA LTD

07 1BARR

08 1CIPLA

09 1CIPLA LIMITED

10 3CIPLA LTD

11 1HEC PHARM

12 1HETERO DRUGS LTD

13 1HETERO LABS LTD III

14 1HETERO LABS UNIT III

15 1HIKMA

16 1LIAONING CHENGDA

17 1LUPIN LTD

18 1MACLEODS PHARMS LTD

19 2MATRIX LABS

20 1MICRO LABS

21 2MYLAN LABS LTD

22 1MYLAN PHARMA

23 2NORVIUM BIOSCIENCE

24 1RANBAXY LABS LTD

25 6VIIV HLTHCARE

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

RLD :

TE Code :

LAMIVUDINE; ZIDOVUDINE; NEVIRAPINE

Brand Name : Lamivudine/Zidovudine 150 mg/300 mg Tablets Co-packaged with Nevirapine 200 mg Tablets

Dosage Form : TABLET; ORAL

Dosage Strength : 150MG; 300MG; 200MG

Approval Date :

Application Number : 21988

RX/OTC/DISCN :

RLD :

TE Code :

Strides Pharma Science

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

RLD :

TE Code :

LAMIVUDINE; NEVIRAPINE; ZIDOVUDINE

Brand Name : LAMIVUDINE; NEVIRAPINE; ZIDOVUDINE

Dosage Form : TABLET; ORAL

Dosage Strength : 150MG; 200MG; 300MG

Approval Date :

Application Number : 22464

RX/OTC/DISCN :

RLD :

TE Code :

Strides Pharma Science

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

RLD :

TE Code :

LAMIVUDINE; NEVIRAPINE; ZIDOVUDINE

Brand Name : LAMIVUDINE; NEVIRAPINE; ZIDOVUDINE

Dosage Form : TABLET, FOR SUSPENSION; ORAL

Dosage Strength : 30MG; 50MG; 60MG

Approval Date :

Application Number : 202685

RX/OTC/DISCN :

RLD :

TE Code :

Strides Pharma Science

04

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

LAMIVUDINE; ZIDOVUDINE; NEVIRAPINE

Brand Name : Lamivudine, Zidovudine, Nevirapine Tabs 150mg/300mg/200mg

Dosage Form : TABLET; ORAL

Dosage Strength : 150MG; 300MG; 200MG

Approval Date :

Application Number : 21939

RX/OTC/DISCN :

RLD :

TE Code :

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05

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

ZIDOVUDINE

Brand Name : RETROVIR

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Approval Date : 1987-03-19

Application Number : 19655

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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06

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

ZIDOVUDINE

Brand Name : RETROVIR

Dosage Form : SOLUTION;ORAL

Dosage Strength : 50MG/5ML

Approval Date : 1989-09-28

Application Number : 19910

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AA

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07

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

ZIDOVUDINE

Brand Name : RETROVIR

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 10MG/ML

Approval Date : 1990-02-02

Application Number : 19951

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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08

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

ZIDOVUDINE

Brand Name : RETROVIR

Dosage Form : TABLET;ORAL

Dosage Strength : 200MG

Approval Date : 1995-12-19

Application Number : 20518

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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09

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

ZIDOVUDINE

Brand Name : RETROVIR

Dosage Form : TABLET;ORAL

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

Approval Date : 1996-10-04

Application Number : 20518

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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10

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

ABACAVIR SULFATE; LAMIVUDINE; ZIDOVUDINE

Brand Name : TRIZIVIR

Dosage Form : TABLET;ORAL

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

Approval Date : 2000-11-14

Application Number : 21205

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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