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01 1Promius Pharma

02 1Skyepharma

03 6Strides Pharma Science

04 62care4

05 22care4 ApS

06 1AHN Pharma

07 1ANI Pharmaceuticals Inc

08 4Accord healthcare

09 4Actavis Inc

10 1Alkermes Plc

11 2Alphapharm PTY Ltd

12 3Apotex Inc

13 2Arrow Pharmaceuticals

14 1Aspire Lifesciences Pvt Ltd

15 10AstraZeneca

16 3Aurobindo Pharma Limited

17 1Avenza Pharmaceuticals

18 4CHIESI USA INC

19 4Centurion Laboratories

20 3Chartwell Pharmaceuticals llc

21 3Chiesi Group

22 6Clinect

23 8DOC Generici

24 4Dexcel Pharma

25 5EG SpA

26 4EG Spa

27 3Farm Agon

28 2GSK

29 1Hanlim Pharmaceuticals Inc

30 3Hikma Pharmaceuticals

31 4IST.LUSOFARMACO D'ITALIA SpA

32 3IVAX Pharmaceuticals Inc

33 3Istituto Lusofarmaco D'Italia

34 1JUNO PHARMACEUTICALS CORP.

35 3Lunan Pharmaceutical

36 1Maxheal Pharmaceuticals (India) Ltd

37 3Merck & Co

38 3Merus Labs Luxco II S.à r.l.

39 5Norgine

40 6ORIFARM GROUP AS

41 2Omnivium Pharmaceuticals

42 1PRO DOC LIMITEE

43 2PRO.MED.CS Praha

44 1Pharma Dynamics

45 2Pharmaco Distribution

46 2Pharmascience Inc.

47 3RICONPHARMA LLC

48 7RIEMSER Pharma GmbH

49 3Ratiopharm GmbH

50 1Recipharm AB

51 6Sandoz B2B

52 1TEDEX Oy

53 1TOPRIDGE PHARMA (IRELAND) LTD

54 2TopRidge Pharma (Ireland) Limited

55 3Torrent Pharmaceuticals Limited

56 7UCB Pharma S.A

57 1Valpharma

58 7Viatris

59 2Yangtze River Pharmaceutical Group

60 3Zim Laboratories

61 3Zydus Lifesciences

62 3Zydus Pharmaceuticals

63 24Blank

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PharmaCompass

01

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ISOSORBIDE MONONITRATE

Brand Name : ISMO

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Packaging :

Approval Date : 1991-12-30

Application Number : 19091

Regulatory Info : DISCN

Registration Country : USA

Dr. Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSkyepharma, an Expert and Innovative CDMO Partner for tailor-made solutions in complex oral solids and bioproduction.

Regulatory Info : DISCN

Registration Country : USA

ISOSORBIDE MONONITRATE

Brand Name : ISOSORBIDE MONONITRATE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 60MG

Packaging :

Approval Date : 1999-10-07

Application Number : 75166

Regulatory Info : DISCN

Registration Country : USA

Skyepharma Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : DISCN

Registration Country : USA

ISOSORBIDE MONONITRATE

Brand Name : ISOSORBIDE MONONITRATE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 2010-08-11

Application Number : 90598

Regulatory Info : DISCN

Registration Country : USA

Strides Pharma Science

04

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : DISCN

Registration Country : USA

ISOSORBIDE MONONITRATE

Brand Name : ISOSORBIDE MONONITRATE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 60MG

Packaging :

Approval Date : 2010-08-11

Application Number : 90598

Regulatory Info : DISCN

Registration Country : USA

Strides Pharma Science

05

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : DISCN

Registration Country : USA

ISOSORBIDE MONONITRATE

Brand Name : ISOSORBIDE MONONITRATE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 120MG

Packaging :

Approval Date : 2010-08-11

Application Number : 90598

Regulatory Info : DISCN

Registration Country : USA

Strides Pharma Science

06

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info :

Registration Country : India

Isosorbide Mononitrate

Brand Name :

Dosage Form : Tablet

Dosage Strength : 30MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

07

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info :

Registration Country : India

Isosorbide Mononitrate

Brand Name :

Dosage Form : Tablet

Dosage Strength : 60MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

08

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info :

Registration Country : India

Isosorbide Mononitrate

Brand Name :

Dosage Form : Tablet

Dosage Strength : 120MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

09

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ISOSORBIDE MONONITRATE

Brand Name : ISOSORBIDE MONONITRATE

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Packaging :

Approval Date : 1998-10-30

Application Number : 75037

Regulatory Info : RX

Registration Country : USA

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10

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ISOSORBIDE MONONITRATE

Brand Name : ISOSORBIDE MONONITRATE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 1998-10-30

Application Number : 75037

Regulatory Info : RX

Registration Country : USA

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11

SupplySide West 2024
Not Confirmed
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SupplySide West 2024
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ISOSORBIDE MONONITRATE

Brand Name : ISOSORBIDE MONONITRATE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 60MG

Packaging :

Approval Date : 1998-09-22

Application Number : 75041

Regulatory Info : DISCN

Registration Country : USA

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12

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Not Confirmed
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ISOSORBIDE MONONITRATE

Brand Name : ISOSORBIDE MONONITRATE

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Packaging :

Approval Date : 1998-11-27

Application Number : 75147

Regulatory Info : DISCN

Registration Country : USA

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13

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ISOSORBIDE MONONITRATE

Brand Name : ISOSORBIDE MONONITRATE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 60MG

Packaging :

Approval Date : 1998-10-30

Application Number : 75155

Regulatory Info : RX

Registration Country : USA

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14

SupplySide West 2024
Not Confirmed
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ISOSORBIDE MONONITRATE

Brand Name : ISOSORBIDE MONONITRATE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 2000-01-13

Application Number : 75155

Regulatory Info : RX

Registration Country : USA

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15

SupplySide West 2024
Not Confirmed
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ISOSORBIDE MONONITRATE

Brand Name : ISOSORBIDE MONONITRATE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 120MG

Packaging :

Approval Date : 2000-08-04

Application Number : 75155

Regulatory Info : RX

Registration Country : USA

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16

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Not Confirmed
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ISOSORBIDE MONONITRATE

Brand Name : IMDUR

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1993-08-12

Application Number : 20225

Regulatory Info : DISCN

Registration Country : USA

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17

SupplySide West 2024
Not Confirmed
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ISOSORBIDE MONONITRATE

Brand Name : IMDUR

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1993-08-12

Application Number : 20225

Regulatory Info : DISCN

Registration Country : USA

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18

SupplySide West 2024
Not Confirmed
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ISOSORBIDE MONONITRATE

Brand Name : IMDUR

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1995-03-30

Application Number : 20225

Regulatory Info : DISCN

Registration Country : USA

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19

SupplySide West 2024
Not Confirmed
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ISOSORBIDE MONONITRATE

Brand Name : MONOKET

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Packaging :

Approval Date : 1993-06-30

Application Number : 20215

Regulatory Info : RX

Registration Country : USA

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20

SupplySide West 2024
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ISOSORBIDE MONONITRATE

Brand Name : MONOKET

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 1993-06-30

Application Number : 20215

Regulatory Info : RX

Registration Country : USA

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