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01 2Dr. Reddy's Laboratories

02 1Taro Pharmaceutical Industries

03 8Strides Pharma Science

04 2Granules India Limited

05 6ANI Pharmaceuticals Inc

06 1Acme Lifetech

07 5Actavis Inc

08 2Ajanta Pharma Limited

09 3Amneal Pharmaceuticals

10 1Amnos Lifesciences

11 2Apofri AB

12 5Apotex Inc

13 2Appco Pharmaceutical Corp

14 5Aurobindo Pharma Limited

15 2Avet Pharmaceuticals

16 1BEDFORD LABS

17 2Boehringer Ingelheim GmbH

18 4Chattem Chemicals, Inc

19 1Contract Pharmacal Corporation

20 2ENDO OPERATIONS

21 1Epic Pharma. LLC.

22 13GSK

23 2Glenmark Pharmaceuticals

24 2Glumex Pharmaceuticals Mfg. Pvt. Ltd

25 1Grupo Columbia

26 2Hikma Pharmaceuticals

27 2Ind Swift Laboratories Limited

28 2Kolmar Korea Co., Ltd.

29 1Kusum Healthcare Pvt Ltd

30 2Lannett Company, Inc.

31 1Lifespan Biotech

32 2MARCAN PHARMACEUTICALS INC

33 2MINT PHARMACEUTICALS INC

34 2Meda OTC AB

35 2Myungmoon Pharm. Co., LTD.

36 5NORVIUM BIOSCIENCE

37 1Nobel Ilac Sanayii Ve Ticaret A.S.

38 4Nostrum Laboratories

39 2Novitium Pharma LLC

40 2ORIFARM GROUP AS

41 3PAI Pharmaceutical Associates

42 1PHARM ASSOC

43 3Perrigo Company plc

44 4Pharmascience Inc.

45 4RANBAXY LABORATORIES LIMITED

46 9Sandoz B2B

47 3Sun Pharmaceutical Industries Limited

48 2THINQ Pharma-CRO PVT Ltd

49 2Teva Pharmaceutical Industries

50 1Theon Pharmaceuticals

51 1Tolmar

52 1Torrent Pharmaceuticals Limited

53 3Umedica Laboratories

54 2VKT Pharma

55 6Viatris

56 2Vista Pharmaceuticals

57 9Wockhardt

58 4XYZ Pharma

59 1Zydus Pharmaceuticals

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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

RANITIDINE HYDROCHLORIDE

Brand Name : RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 2005-07-27

Application Number : 76705

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : DISCN

Registration Country : USA

RANITIDINE HYDROCHLORIDE

Brand Name : RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 2011-06-28

Application Number : 200536

Regulatory Info : DISCN

Registration Country : USA

Strides Pharma Science

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

Regulatory Info : DISCN

Registration Country : USA

RANITIDINE HYDROCHLORIDE

Brand Name : RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 2018-08-20

Application Number : 210243

Regulatory Info : DISCN

Registration Country : USA

Granules India

04

  • 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

RANITIDINE HYDROCHLORIDE

Brand Name : RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 300MG BASE

Packaging :

Approval Date : 2005-07-27

Application Number : 76705

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

05

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CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : RANITIDINE HYDROCHLORIDE

Dosage Form : SYRUP;ORAL

Dosage Strength : EQ 15MG BASE/ML

Packaging :

Approval Date : 2011-06-13

Application Number : 77476

Regulatory Info : DISCN

Registration Country : USA

blank

06

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : DISCN

Registration Country : USA

RANITIDINE HYDROCHLORIDE

Brand Name : RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 75MG BASE

Packaging :

Approval Date : 2012-02-29

Application Number : 201745

Regulatory Info : DISCN

Registration Country : USA

Strides Pharma Science

07

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : DISCN

Registration Country : USA

RANITIDINE HYDROCHLORIDE

Brand Name : RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 2016-08-22

Application Number : 205512

Regulatory Info : DISCN

Registration Country : USA

Strides Pharma Science

08

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : DISCN

Registration Country : USA

RANITIDINE HYDROCHLORIDE

Brand Name : RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 300MG BASE

Packaging :

Approval Date : 2016-08-22

Application Number : 205512

Regulatory Info : DISCN

Registration Country : USA

Strides Pharma Science

09

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : DISCN

Registration Country : USA

RANITIDINE HYDROCHLORIDE

Brand Name : RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 75MG BASE

Packaging :

Approval Date : 2018-03-05

Application Number : 209160

Regulatory Info : DISCN

Registration Country : USA

Strides Pharma Science

10

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : DISCN

Registration Country : USA

RANITIDINE HYDROCHLORIDE

Brand Name : RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 2018-02-22

Application Number : 209161

Regulatory Info : DISCN

Registration Country : USA

Strides Pharma Science

11

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : DISCN

Registration Country : USA

RANITIDINE HYDROCHLORIDE

Brand Name : RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 2018-08-01

Application Number : 210010

Regulatory Info : DISCN

Registration Country : USA

Strides Pharma Science

12

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : DISCN

Registration Country : USA

RANITIDINE HYDROCHLORIDE

Brand Name : RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 300MG BASE

Packaging :

Approval Date : 2018-08-01

Application Number : 210010

Regulatory Info : DISCN

Registration Country : USA

Strides Pharma Science

13

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

Regulatory Info : DISCN

Registration Country : USA

RANITIDINE HYDROCHLORIDE

Brand Name : RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 2018-08-20

Application Number : 210243

Regulatory Info : DISCN

Registration Country : USA

Granules India

14

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : ZANTAC 75

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 75MG BASE

Packaging :

Approval Date : 1995-12-19

Application Number : 20520

Regulatory Info : DISCN

Registration Country : USA

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15

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : ZANTAC 75

Dosage Form : TABLET, EFFERVESCENT;ORAL

Dosage Strength : EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1998-02-26

Application Number : 20745

Regulatory Info : DISCN

Registration Country : USA

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16

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : ZANTAC 150

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 2004-08-31

Application Number : 21698

Regulatory Info : DISCN

Registration Country : USA

blank

17

CPhI India 2024
Not Confirmed
arrow
arrow
CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : ZANTAC 150

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 2007-03-13

Application Number : 21698

Regulatory Info : DISCN

Registration Country : USA

blank

18

CPhI India 2024
Not Confirmed
arrow
arrow
CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : ZANTAC 150

Dosage Form : TABLET;ORAL

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

Packaging :

Approval Date : 1983-06-09

Application Number : 18703

Regulatory Info : DISCN

Registration Country : USA

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19

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : ZANTAC 300

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 : 1985-12-09

Application Number : 18703

Regulatory Info : DISCN

Registration Country : USA

blank

20

CPhI India 2024
Not Confirmed
arrow
arrow
CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : ZANTAC

Dosage Form : SYRUP;ORAL

Dosage Strength : EQ 15MG BASE/ML

Packaging :

Approval Date : 1988-12-30

Application Number : 19675

Regulatory Info : DISCN

Registration Country : USA

blank

21

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : ZANTAC 150

Dosage Form : CAPSULE;ORAL

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

Packaging :

Approval Date : 1994-03-08

Application Number : 20095

Regulatory Info : DISCN

Registration Country : USA

blank

22

CPhI India 2024
Not Confirmed
arrow
arrow
CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : ZANTAC 300

Dosage Form : CAPSULE;ORAL

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

Packaging :

Approval Date : 1994-03-08

Application Number : 20095

Regulatory Info : DISCN

Registration Country : USA

blank

23

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : ZANTAC 150

Dosage Form : TABLET, EFFERVESCENT;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 1994-03-31

Application Number : 20251

Regulatory Info : DISCN

Registration Country : USA

blank

24

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : ZANTAC 150

Dosage Form : GRANULE, EFFERVESCENT;ORAL

Dosage Strength : EQ 150MG BASE/PACKET

Packaging :

Approval Date : 1994-03-31

Application Number : 20251

Regulatory Info : DISCN

Registration Country : USA

blank

25

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : ZANTAC 25

Dosage Form : TABLET, EFFERVESCENT;ORAL

Dosage Strength : EQ 25MG BASE

Packaging :

Approval Date : 2004-04-01

Application Number : 20251

Regulatory Info : DISCN

Registration Country : USA

blank

26

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : ZANTAC

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 25MG BASE/ML

Packaging :

Approval Date : 1984-10-19

Application Number : 19090

Regulatory Info : DISCN

Registration Country : USA

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27

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : ZANTAC IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 50MG BASE/100ML

Packaging :

Approval Date : 1986-12-17

Application Number : 19593

Regulatory Info : DISCN

Registration Country : USA

blank

28

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : ZANTAC IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/ML

Packaging :

Approval Date : 1991-09-27

Application Number : 19593

Regulatory Info : DISCN

Registration Country : USA

blank

29

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 1997-08-22

Application Number : 74023

Regulatory Info : DISCN

Registration Country : USA

blank

30

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 300MG BASE

Packaging :

Approval Date : 1997-08-22

Application Number : 74023

Regulatory Info : DISCN

Registration Country : USA

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