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01 1Octavius Pharma Pvt. Ltd

02 2Pharmathen SA

03 1AGIPS FARMACEUTICI Srl

04 1ALMUS Srl

05 2ANGITA PHARMA INC.

06 2Abdi Ibrahim

07 8Accord healthcare

08 8Actavis Inc

09 2Alphapharm PTY Ltd

10 9Apotex Inc

11 2Auro Pharma Inc

12 5Aurobindo Pharma Limited

13 1BRUNO FARMACEUTICI SpA

14 2Blue Fish Solvay AB

15 9Chartwell Pharmaceuticals llc

16 5Cipla

17 1DOC Generici

18 1EG SpA

19 1EPIFARMA Srl

20 1Ebb Medical

21 1FG Srl

22 1Farm Agon

23 1Flagship Biotech International Pvt. Ltd

24 1Halewood Laboratories Pvt. Ltd

25 4Hangzhou Minsheng Binjiang Pharmaceutical CO., Ltd

26 1Hikma Pharmaceuticals

27 1IBN Savio

28 1IFA SA Laboratories

29 1IST.CHIM.INTERNAZ. RENDE Srl

30 5Impax Laboratories

31 1Infugen Pharma

32 3Intas Pharmaceuticals

33 4Ipca Laboratories

34 1JAMP PHARMA

35 4Jubilant Cadista Pharmaceuticals

36 1Kusum Healthcare Pvt Ltd

37 1LABORATOIRE RIVA INC.

38 2Laboratoires Teriak TN

39 2Laboratorios Alter

40 1Loxim Industries

41 1MANTRA PHARMA INC

42 1MINT PHARMACEUTICALS INC

43 1MS Pharma

44 2Medipha Sante

45 11Merck & Co

46 2Myungmoon Pharm. Co., LTD.

47 1NEAPHARMA Srl

48 4NEOPHARMED GENTILI Srl

49 1Nora Pharma

50 1Novitium Pharma LLC

51 1ORGANON CANADA INC.

52 15Organon

53 1Organon South Africa (Pty) Ltd

54 1PRO DOC LIMITEE

55 1Pensa Pharma

56 1Pharmacare Premium

57 3Pharmascience Inc.

58 1Radius Health

59 1Ratiopharm GmbH

60 4Rising Pharmaceuticals Inc

61 4S.F.GROUP Srl

62 1SANIS HEALTH INC

63 2SIGMA TAU

64 1SIVEM PHARMACEUTICALS ULC

65 1SO.SE.PHARM Srl

66 2STADA Arzneimittel

67 6Sandoz B2B

68 5Sun Pharmaceutical Industries Limited

69 1TECNIGEN Srl

70 6Teva Pharmaceutical Industries

71 2Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories Sa

72 7Viatris

73 2WAGNER PHARMACEUTICALS PTY LTD

74 1World Medicine

75 1XL Laboratories Private Limited

76 1Yangtze River Pharmaceutical Group

77 1Zentiva

78 6Zim Laboratories

79 40Blank

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothOctavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.

Regulatory Info :

Registration Country : India

Alendronate Sodium

Brand Name : Alendronate Sodium

Dosage Form : DC Granules

Dosage Strength : 70MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Octavius Pharma

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.

Regulatory Info : EU Approved

Registration Country : Greece

Alendronate Sodium; Vitamin D3

Brand Name :

Dosage Form : Tablet

Dosage Strength : 70MG; 2800IU

Packaging :

Approval Date :

Application Number :

Regulatory Info : EU Approved

Registration Country : Greece

Pharmathen

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.

Regulatory Info : EU Approved

Registration Country : Greece

Alendronate Sodium; Vitamin D3

Brand Name :

Dosage Form : Tablet

Dosage Strength : 70MG; 5600IU

Packaging :

Approval Date :

Application Number :

Regulatory Info : EU Approved

Registration Country : Greece

Pharmathen

04

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2009-04-22

Application Number : 75871

Regulatory Info : DISCN

Registration Country : USA

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05

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2009-04-22

Application Number : 75871

Regulatory Info : DISCN

Registration Country : USA

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06

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 40MG BASE

Packaging :

Approval Date : 2009-04-22

Application Number : 75871

Regulatory Info : DISCN

Registration Country : USA

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07

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 35MG BASE

Packaging :

Approval Date : 2009-04-22

Application Number : 75871

Regulatory Info : DISCN

Registration Country : USA

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08

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2008-02-06

Application Number : 75710

Regulatory Info : DISCN

Registration Country : USA

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09

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2008-02-06

Application Number : 75710

Regulatory Info : DISCN

Registration Country : USA

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10

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 35MG BASE

Packaging :

Approval Date : 2008-02-06

Application Number : 75710

Regulatory Info : DISCN

Registration Country : USA

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11

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 40MG BASE

Packaging :

Approval Date : 2008-02-06

Application Number : 75710

Regulatory Info : DISCN

Registration Country : USA

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12

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 70MG BASE

Packaging :

Approval Date : 2008-02-06

Application Number : 75710

Regulatory Info : DISCN

Registration Country : USA

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13

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM

Brand Name : FOSAMAX

Dosage Form : SOLUTION;ORAL

Dosage Strength : EQ 70MG BASE/75ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2003-09-17

Application Number : 21575

Regulatory Info : DISCN

Registration Country : USA

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14

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM

Brand Name : FOSAMAX

Dosage Form : TABLET;ORAL

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

Packaging :

Approval Date : 1995-09-29

Application Number : 20560

Regulatory Info : DISCN

Registration Country : USA

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15

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM

Brand Name : FOSAMAX

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1995-09-29

Application Number : 20560

Regulatory Info : DISCN

Registration Country : USA

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16

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM

Brand Name : FOSAMAX

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1997-04-25

Application Number : 20560

Regulatory Info : DISCN

Registration Country : USA

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17

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM

Brand Name : FOSAMAX

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 35MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2000-10-20

Application Number : 20560

Regulatory Info : DISCN

Registration Country : USA

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18

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM

Brand Name : FOSAMAX

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 70MG BASE

Packaging :

Approval Date : 2000-10-20

Application Number : 20560

Regulatory Info : RX

Registration Country : USA

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19

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM; CHOLECALCIFEROL

Brand Name : FOSAMAX PLUS D

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 70MG BASE;2,800 IU

Packaging :

Approval Date : 2005-04-07

Application Number : 21762

Regulatory Info : RX

Registration Country : USA

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20

OPRD
Not Confirmed
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OPRD
Not Confirmed

ALENDRONATE SODIUM; CHOLECALCIFEROL

Brand Name : FOSAMAX PLUS D

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 70MG BASE;5,600 IU

Packaging :

Approval Date : 2007-04-26

Application Number : 21762

Regulatory Info : RX

Registration Country : USA

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