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01 3Dr. Reddy's Laboratories

02 1Taro Pharmaceutical Industries

03 2Adcock Ingram

04 1American Regent

05 3Amneal Pharmaceuticals

06 2Apotex Inc

07 3Aurobindo Pharma Limited

08 1Barr Laboratories

09 3Baxter Healthcare Corporation

10 3Bionpharma

11 2Bluefish Pharmaceuticals AB

12 1Chartwell Pharmaceuticals llc

13 2Epic Pharma. LLC.

14 10F. Hoffmann-La Roche

15 4Farbe Firma

16 2Flagship Biotech International Pvt. Ltd

17 1Fresenius Kabi AB Brunna

18 3Fresenius Kabi USA

19 1Ha Noi CPC1 Pharmaceutical JSC

20 1Hameln Pharma GmbH

21 7Hikma Pharmaceuticals

22 1Igenius Life Sciences

23 1Intra-Sana Laboratories

24 1JAMP PHARMA

25 3NORVIUM BIOSCIENCE

26 2Natco Pharma

27 1Natco Pharma (Canada) Inc

28 1Omega Laboratories Limited

29 1OrBion Pharmaceuticals

30 2Pluviaendo

31 2Rising Pharmaceuticals Inc

32 2STADA Arzneimittel

33 6Sandoz B2B

34 2Teva Pharmaceutical Industries

35 4Viatris

36 3Wockhardt

37 4XYZ Pharma

38 1Yangtze River Pharmaceutical Group

39 3Yung Shin Pharmaceutical Industrial

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : DISCN

Registration Country : USA

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE PRESERVATIVE FREE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/ML (EQ 1MG BASE/ML)

Packaging :

Approval Date : 2007-12-31

Application Number : 77165

Regulatory Info : DISCN

Registration Country : USA

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : RX

Registration Country : USA

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML)

Packaging :

Approval Date : 2008-06-30

Application Number : 77297

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : RX

Registration Country : USA

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)

Packaging :

Approval Date : 2007-12-31

Application Number : 78392

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

04

arrow
Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2010-05-28

Application Number : 90817

Regulatory Info : RX

Registration Country : USA

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05

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/ML (EQ 1MG BASE/ML)

Packaging :

Approval Date : 2008-06-30

Application Number : 78258

Regulatory Info : RX

Registration Country : USA

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06

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML)

Packaging :

Approval Date : 2008-06-30

Application Number : 78258

Regulatory Info : RX

Registration Country : USA

blank

07

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)

Packaging :

Approval Date : 2007-12-31

Application Number : 78262

Regulatory Info : RX

Registration Country : USA

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08

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2007-12-31

Application Number : 78221

Regulatory Info : DISCN

Registration Country : USA

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09

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)

Packaging :

Approval Date : 2007-12-31

Application Number : 78197

Regulatory Info : DISCN

Registration Country : USA

blank

10

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/ML (EQ 1MG BASE/ML)

Packaging :

Approval Date : 2008-06-30

Application Number : 78198

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

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML)

Packaging :

Approval Date : 2008-06-30

Application Number : 78198

Regulatory Info : DISCN

Registration Country : USA

blank

12

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2008-02-27

Application Number : 78037

Regulatory Info : RX

Registration Country : USA

blank

13

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2007-12-31

Application Number : 78260

Regulatory Info : DISCN

Registration Country : USA

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14

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : KYTRIL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 3MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1993-12-29

Application Number : 20239

Regulatory Info : DISCN

Registration Country : USA

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15

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : KYTRIL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1994-03-11

Application Number : 20239

Regulatory Info : DISCN

Registration Country : USA

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16

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : KYTRIL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2004-09-17

Application Number : 20239

Regulatory Info : DISCN

Registration Country : USA

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17

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : KYTRIL

Dosage Form : INJECTABLE;INJECTION

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

Packaging :

Approval Date : 1994-03-11

Application Number : 20239

Regulatory Info : DISCN

Registration Country : USA

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18

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : KYTRIL

Dosage Form : TABLET;ORAL

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

Packaging :

Approval Date : 1995-03-16

Application Number : 20305

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

GRANISETRON HYDROCHLORIDE

Brand Name : KYTRIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE **Federal Register determination that product was not withdrawn or discontinued for safety or effectiveness reasons**

Packaging :

Approval Date : 1998-06-15

Application Number : 20305

Regulatory Info : DISCN

Registration Country : USA

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20

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : KYTRIL

Dosage Form : SOLUTION;ORAL

Dosage Strength : EQ 2MG BASE/10ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2001-06-27

Application Number : 21238

Regulatory Info : DISCN

Registration Country : USA

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21

Fi Europe 2024
Not Confirmed
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arrow
Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML)

Packaging :

Approval Date : 2008-06-30

Application Number : 78090

Regulatory Info : RX

Registration Country : USA

blank

22

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE PRESERVATIVE FREE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/ML (EQ 1MG BASE/ML)

Packaging :

Approval Date : 2008-06-30

Application Number : 78096

Regulatory Info : RX

Registration Country : USA

blank

23

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML)

Packaging :

Approval Date : 2007-12-31

Application Number : 77177

Regulatory Info : RX

Registration Country : USA

blank

24

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML)

Packaging :

Approval Date : 2008-06-30

Application Number : 77186

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

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/ML (EQ 1MG BASE/ML)

Packaging :

Approval Date : 2008-06-30

Application Number : 77187

Regulatory Info : RX

Registration Country : USA

blank

26

Fi Europe 2024
Not Confirmed
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arrow
Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2007-12-31

Application Number : 77842

Regulatory Info : DISCN

Registration Country : USA

blank

27

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)

Packaging :

Approval Date : 2008-06-26

Application Number : 77913

Regulatory Info : RX

Registration Country : USA

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28

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISOL

Dosage Form : SOLUTION;ORAL

Dosage Strength : EQ 2MG BASE/10ML

Packaging :

Approval Date : 2008-02-28

Application Number : 78334

Regulatory Info : DISCN

Registration Country : USA

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29

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/ML (EQ 1MG BASE/ML)

Packaging :

Approval Date : 2008-01-03

Application Number : 77963

Regulatory Info : DISCN

Registration Country : USA

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30

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

GRANISETRON HYDROCHLORIDE

Brand Name : GRANISETRON HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2007-12-31

Application Number : 78080

Regulatory Info : DISCN

Registration Country : USA

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