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01 2Dr. Reddy's Laboratories

02 8Strides Pharma Science

03 2Granules India Limited

04 6ANI Pharmaceuticals Inc

05 1Acme Lifetech

06 5Actavis Inc

07 2Ajanta Pharma Limited

08 3Amneal Pharmaceuticals

09 1Amnos Lifesciences

10 2Apofri AB

11 5Apotex Inc

12 2Appco Pharmaceutical Corp

13 5Aurobindo Pharma Limited

14 2Avet Pharmaceuticals

15 1BEDFORD LABS

16 2Boehringer Ingelheim GmbH

17 4Chattem Chemicals, Inc

18 1Contract Pharmacal Corporation

19 2ENDO OPERATIONS

20 1Epic Pharma. LLC.

21 13GSK

22 2Glenmark Pharmaceuticals

23 2Glumex Pharmaceuticals Mfg. Pvt. Ltd

24 1Grupo Columbia

25 2Hikma Pharmaceuticals

26 2Ind Swift Laboratories Limited

27 2Kolmar Korea Co., Ltd.

28 1Kusum Healthcare Pvt Ltd

29 2Lannett Company, Inc.

30 1Lifespan Biotech

31 2MARCAN PHARMACEUTICALS INC

32 2MINT PHARMACEUTICALS INC

33 2Meda OTC AB

34 2Myungmoon Pharm. Co., LTD.

35 5NORVIUM BIOSCIENCE

36 1Nobel Ilac Sanayii Ve Ticaret A.S.

37 4Nostrum Laboratories

38 2Novitium Pharma LLC

39 2ORIFARM GROUP AS

40 3PAI Pharmaceutical Associates

41 1PHARM ASSOC

42 3Perrigo Company plc

43 5Pharmascience Inc.

44 4RANBAXY LABORATORIES LIMITED

45 9Sandoz B2B

46 3Sun Pharmaceutical Industries Limited

47 2THINQ Pharma-CRO PVT Ltd

48 1Taro Pharmaceutical Industries

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

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PharmaVenue
Not Confirmed
  • 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

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PharmaVenue
Not Confirmed
  • 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

arrow
PharmaVenue
Not Confirmed
  • 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

06

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PharmaVenue
Not Confirmed
  • 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

07

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PharmaVenue
Not Confirmed
  • 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

08

arrow
PharmaVenue
Not Confirmed
  • 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

09

arrow
PharmaVenue
Not Confirmed
  • 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

10

arrow
PharmaVenue
Not Confirmed
  • 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

11

arrow
PharmaVenue
Not Confirmed
  • 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

12

arrow
PharmaVenue
Not Confirmed
  • 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

13

PharmaVenue
Not Confirmed
arrow
arrow
PharmaVenue
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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14

PharmaVenue
Not Confirmed
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PharmaVenue
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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15

PharmaVenue
Not Confirmed
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PharmaVenue
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

16

PharmaVenue
Not Confirmed
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PharmaVenue
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

17

PharmaVenue
Not Confirmed
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PharmaVenue
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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18

PharmaVenue
Not Confirmed
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PharmaVenue
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

19

PharmaVenue
Not Confirmed
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PharmaVenue
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

20

PharmaVenue
Not Confirmed
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PharmaVenue
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

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21

PharmaVenue
Not Confirmed
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PharmaVenue
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

22

PharmaVenue
Not Confirmed
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PharmaVenue
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

23

PharmaVenue
Not Confirmed
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PharmaVenue
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

24

PharmaVenue
Not Confirmed
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PharmaVenue
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

25

PharmaVenue
Not Confirmed
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PharmaVenue
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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26

PharmaVenue
Not Confirmed
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PharmaVenue
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

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27

PharmaVenue
Not Confirmed
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PharmaVenue
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

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28

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

RANITIDINE HYDROCHLORIDE

Brand Name : RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 1997-08-29

Application Number : 74467

Regulatory Info : RX

Registration Country : USA

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29

PharmaVenue
Not Confirmed
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PharmaVenue
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

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30

PharmaVenue
Not Confirmed
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PharmaVenue
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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