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01 4Naprod Life Sciences

02 2NanoAlvand

03 2Supriya Lifescience

04 31Accord healthcare

05 2Accure Labs

06 12Actavis Inc

07 2American Regent

08 3Apotex Inc

09 3AqVida GmbH

10 6Aurobindo Pharma Limited

11 2Cipla Medpro South Africa

12 10Eli Lilly

13 2Emcure Pharmaceuticals

14 2Eriochem S.A.

15 2Eurolab

16 2Flagship Biotech International Pvt. Ltd

17 10Fresenius Kabi AB Brunna

18 3Fresenius Kabi Oncology Limited

19 6Fresenius Kabi USA

20 2Fresenius SE & Co. KGaA

21 2GLAND PHARMA LIMITED

22 3GetWell Pharmaceutical

23 3Grupo Azevedos

24 2Hameln rds

25 2Hansoh Pharma

26 1Health Biotech

27 6Hikma Pharmaceuticals

28 13Hospira, Inc.

29 3Jodas Expoim Pvt. Ltd

30 1Kremedine Health

31 3Meitheal Pharmaceuticals

32 3NORVIUM BIOSCIENCE

33 3Nishchay Pharmaceuticals Pvt. Ltd.

34 3Novast Laboratories

35 2Panacea Biotec Limited

36 4Pfizer Consumer Healthcare

37 1Pfizer Inc

38 2RANBAXY LABORATORIES LIMITED

39 1STADA Arzneimittel

40 5Sagent Pharmaceuticals

41 2Sakar Healthcare

42 2Samyang Biopharmaceuticals

43 15Sandoz B2B

44 5Shilpa Medicare

45 21Sun Pharmaceutical Industries Limited

46 11Teva Pharmaceutical Industries

47 2Teyro Labs

48 4TherDose Pharma

49 4Viatris

50 1Vinkem Labs Ltd

51 3XYZ Pharma

52 2Xixia Pharmaceuticals (Pty) Ltd

53 2Zydus Lifesciences

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNaprod is a top player in Oncology & Anesthesia FDF through excellent innovation, discovery of new processes & high-quality production.

Regulatory Info :

Registration Country : India

Gemcitabine Hydrochloride

Brand Name :

Dosage Form : Lyophilised Injection

Dosage Strength : 200MG/Vial

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Naprod Life Sciences

02

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

Virtual BoothNanoAlvand is the entrance to Global Markets as a trusted Highly Potent Products manufacturer.

Regulatory Info :

Registration Country : Iran

Gemcitabine

Brand Name : Tiagem

Dosage Form : Vial

Dosage Strength : 200MG/2ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Iran

NanoAlvand

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSupriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.

Regulatory Info :

Registration Country : India

Gemcitabine

Brand Name :

Dosage Form : Injection

Dosage Strength : 200MG/2ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Supriya

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNaprod is a top player in Oncology & Anesthesia FDF through excellent innovation, discovery of new processes & high-quality production.

Regulatory Info :

Registration Country : India

Gemcitabine Hydrochloride

Brand Name :

Dosage Form : Lyophilised Injection

Dosage Strength : 1G/Vial

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Naprod Life Sciences

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNaprod is a top player in Oncology & Anesthesia FDF through excellent innovation, discovery of new processes & high-quality production.

Regulatory Info :

Registration Country : India

Gemcitabine Hydrochloride

Brand Name :

Dosage Form : Lyophilised Injection

Dosage Strength : 1.4G/Vial

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Naprod Life Sciences

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNaprod is a top player in Oncology & Anesthesia FDF through excellent innovation, discovery of new processes & high-quality production.

Regulatory Info :

Registration Country : India

Gemcitabine Hydrochloride

Brand Name :

Dosage Form : Liquid Injection

Dosage Strength : 10MG/ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Naprod Life Sciences

07

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

Virtual BoothNanoAlvand is the entrance to Global Markets as a trusted Highly Potent Products manufacturer.

Regulatory Info :

Registration Country : Iran

Gemcitabine

Brand Name : Tiagem

Dosage Form : Vial

Dosage Strength : 1000MG/10ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Iran

NanoAlvand

08

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSupriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.

Regulatory Info :

Registration Country : India

Gemcitabine

Brand Name :

Dosage Form : Injection

Dosage Strength : 100MG/ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Supriya

09

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 200MG BASE/VIAL

Packaging :

Approval Date : 2011-07-25

Application Number : 79160

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

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 2011-07-25

Application Number : 79160

Regulatory Info : DISCN

Registration Country : USA

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11

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 2016-07-28

Application Number : 79160

Regulatory Info : DISCN

Registration Country : USA

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12

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMZAR

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 200MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1996-05-15

Application Number : 20509

Regulatory Info : DISCN

Registration Country : USA

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13

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMZAR

Dosage Form : INJECTABLE;INJECTION

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

Packaging :

Approval Date : 1996-05-15

Application Number : 20509

Regulatory Info : DISCN

Registration Country : USA

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14

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE; INJECTION

Dosage Strength : EQ 200MG BASE/VIAL

Packaging :

Approval Date :

Application Number : 90242

Regulatory Info :

Registration Country : USA

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15

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE; INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date :

Application Number : 90242

Regulatory Info :

Registration Country : USA

blank

16

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 2011-05-16

Application Number : 90242

Regulatory Info : RX

Registration Country : USA

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17

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 200MG BASE/VIAL

Packaging :

Approval Date : 2011-07-25

Application Number : 90799

Regulatory Info : RX

Registration Country : USA

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18

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 200MG BASE/VIAL

Packaging :

Approval Date : 2012-09-10

Application Number : 90663

Regulatory Info : DISCN

Registration Country : USA

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19

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 2012-09-10

Application Number : 90663

Regulatory Info : DISCN

Registration Country : USA

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20

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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GEMCITABINE

Brand Name : GEMCITABINE

Dosage Form : INJECTABLE; INJECTION

Dosage Strength : 200MG

Packaging :

Approval Date :

Application Number : 78460

Regulatory Info :

Registration Country : USA

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21

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 200MG BASE/VIAL

Packaging :

Approval Date : 2011-07-25

Application Number : 78339

Regulatory Info : RX

Registration Country : USA

blank

22

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 2011-07-25

Application Number : 78339

Regulatory Info : RX

Registration Country : USA

blank

23

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 2010-11-15

Application Number : 79183

Regulatory Info : RX

Registration Country : USA

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24

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 200MG BASE/VIAL

Packaging :

Approval Date : 2011-07-25

Application Number : 78433

Regulatory Info : RX

Registration Country : USA

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25

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 2011-07-25

Application Number : 78433

Regulatory Info : RX

Registration Country : USA

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26

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 2011-01-25

Application Number : 77983

Regulatory Info : DISCN

Registration Country : USA

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27

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 200MG BASE/VIAL

Packaging :

Approval Date : 2011-01-25

Application Number : 77983

Regulatory Info : DISCN

Registration Country : USA

blank

28

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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GEMCITABINE

Brand Name : GEMCITABINE

Dosage Form : INJECTABLE; INJECTION

Dosage Strength : 2G

Packaging :

Approval Date :

Application Number : 90644

Regulatory Info :

Registration Country : USA

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29

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 200MG BASE/VIAL

Packaging :

Approval Date : 2011-07-25

Application Number : 78759

Regulatory Info : RX

Registration Country : USA

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30

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GEMCITABINE HYDROCHLORIDE

Brand Name : GEMCITABINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 2011-07-25

Application Number : 78759

Regulatory Info : RX

Registration Country : USA

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