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01 3Dr. Reddy's Laboratories

02 1Polfa Tarchomin

03 1NanoAlvand

04 1Supriya Lifescience

05 14Accord Healthcare Pty. Ltd.

06 3Accord healthcare

07 1Actavis Inc

08 1Amneal Pharmaceuticals

09 1Aurobindo Pharma Limited

10 2Bristol Laboratories Ltd

11 8Bristol Myers Squibb

12 3Celgene Corporation

13 1CinnaGen Co

14 1Cipla

15 1DR REDDY'S LABORATORIES LTD

16 14Dr Reddy's Laboratories (Australia) Pty Ltd

17 1Dr Reddy's Laboratories (Pty) Ltd

18 14EUGIA PHARMA (AUSTRALIA) PTY LTD

19 1Fresenius Kabi Austria

20 1GetWell Pharmaceutical

21 1HETERO LABS LTD VI

22 1Hainan Poly Pharm

23 1Hansoh Pharma

24 2Hikma Pharmaceuticals

25 1Ideogen AG

26 1JAMP PHARMA

27 1Jodas Expoim Pvt. Ltd

28 28Juno Pharmaceuticals Pty Ltd

29 1Key Oncologics

30 1Lupin Ltd

31 1MSN Laboratories

32 1Meitheal Pharmaceuticals

33 1NORVIUM BIOSCIENCE

34 1Natco Pharma

35 1ORIFARM GROUP AS

36 1Panacea Biotec Limited

37 1SEACROSS PHARMACEUTICALS

38 1Sakar Healthcare

39 2Samyang Biopharmaceuticals

40 16Sandoz B2B

41 1Shilpa Medicare

42 3Spirig Healthcare

43 1Sun Pharmaceutical Industries Limited

44 14Teva Pharma Australia

45 2TherDose Pharma

46 1Vama Lifecare

47 2Viatris

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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 : RX

Registration Country : USA

AZACITIDINE

Brand Name : AZACITIDINE

Dosage Form : POWDER;INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date : 2013-09-16

Application Number : 201537

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

Regulatory Info : Dossier Available

Registration Country : Poland

Azacitidine

Brand Name :

Dosage Form : Powder for Solution for Injection

Dosage Strength : 100MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : Dossier Available

Registration Country : Poland

Polfa Tarchomin

03

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info :

Registration Country : Iran

Azacitidine

Brand Name : Leukaza

Dosage Form : Vial

Dosage Strength : 100MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Iran

NanoAlvand

04

  • 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

Azacitidine

Brand Name :

Dosage Form : Injection

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Supriya

05

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : Lead Market Dossiers- Filed

Registration Country : India

Azacitidine

Brand Name :

Dosage Form : Injection

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date :

Application Number :

Regulatory Info : Lead Market Dossiers- Filed

Registration Country : India

Dr Reddy Company Banner

06

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : Lead Market Dossiers- Approved in both US & EU

Registration Country : India

Azacitidine

Brand Name :

Dosage Form : Injection

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date :

Application Number :

Regulatory Info : Lead Market Dossiers- Approved in both US & EU

Registration Country : India

Dr Reddy Company Banner

07

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

AZACITIDINE

Brand Name : AZACITIDINE

Dosage Form : POWDER;INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date : 2018-07-02

Application Number : 207475

Regulatory Info : RX

Registration Country : USA

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08

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

AZACITIDINE

Brand Name : AZACITIDINE

Dosage Form : POWDER;INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date : 2016-04-29

Application Number : 208216

Regulatory Info : RX

Registration Country : USA

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09

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

AZACITIDINE

Brand Name : AZACITIDINE

Dosage Form : POWDER;INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date : 2022-02-03

Application Number : 211549

Regulatory Info : RX

Registration Country : USA

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10

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

AZACITIDINE

Brand Name : ONUREG

Dosage Form : TABLET;ORAL

Dosage Strength : 200MG

Packaging :

Approval Date : 2020-09-01

Application Number : 214120

Regulatory Info : RX

Registration Country : USA

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11

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

AZACITIDINE

Brand Name : ONUREG

Dosage Form : TABLET;ORAL

Dosage Strength : 300MG

Packaging :

Approval Date : 2020-09-01

Application Number : 214120

Regulatory Info : RX

Registration Country : USA

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12

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

AZACITIDINE

Brand Name : VIDAZA

Dosage Form : POWDER;INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date : 2004-05-19

Application Number : 50794

Regulatory Info : RX

Registration Country : USA

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13

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

AZACITIDINE

Brand Name : AZACITIDINE

Dosage Form : POWDER;INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date : 2018-05-04

Application Number : 209540

Regulatory Info : RX

Registration Country : USA

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14

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

AZACITIDINE

Brand Name : AZACITIDINE

Dosage Form : POWDER;INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date : 2020-06-08

Application Number : 209337

Regulatory Info : RX

Registration Country : USA

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15

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

AZACITIDINE

Brand Name : AZACITIDINE

Dosage Form : POWDER;INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date : 2019-02-27

Application Number : 210748

Regulatory Info : DISCN

Registration Country : USA

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16

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

AZACITIDINE

Brand Name : AZACITIDINE

Dosage Form : POWDER;INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date : 2020-11-02

Application Number : 212128

Regulatory Info : RX

Registration Country : USA

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17

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

AZACITIDINE

Brand Name : AZACITIDINE

Dosage Form : POWDER;INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date : 2024-05-16

Application Number : 212580

Regulatory Info : RX

Registration Country : USA

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18

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

AZACITIDINE

Brand Name : AZACITIDINE

Dosage Form : POWDER;INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date : 2017-06-23

Application Number : 207234

Regulatory Info : RX

Registration Country : USA

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19

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

AZACITIDINE

Brand Name : AZACITIDINE

Dosage Form : POWDER;INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date : 2016-09-29

Application Number : 207518

Regulatory Info : RX

Registration Country : USA

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20

NORVIUM BIOSCIENCE

Country
AACR Annual meeting
Not Confirmed
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NORVIUM BIOSCIENCE

Country
arrow
AACR Annual meeting
Not Confirmed

AZACITIDINE

Brand Name : AZACITIDINE

Dosage Form : POWDER;INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date : 2016-04-28

Application Number : 204949

Regulatory Info : DISCN

Registration Country : USA

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