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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 3Abiogen Pharma S.p.A

08 6Accord healthcare

09 8Actavis Inc

10 2Alphapharm PTY Ltd

11 9Apotex Inc

12 2Auro Pharma Inc

13 5Aurobindo Pharma Limited

14 1BRUNO FARMACEUTICI SpA

15 2Blue Fish Solvay AB

16 9Chartwell Pharmaceuticals llc

17 5Cipla

18 1DOC Generici

19 1EG SpA

20 1EPIFARMA Srl

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 2JAMP PHARMA

35 4Jubilant Cadista Pharmaceuticals

36 1Kusum Healthcare Pvt Ltd

37 1LABORATOIRE RIVA INC.

38 2Laboratoires Teriak TN

39 2Laboratorios Alter

40 1MANTRA PHARMA INC

41 1MINT PHARMACEUTICALS INC

42 1MS Pharma

43 11Merck & Co

44 2Myungmoon Pharm. Co., LTD.

45 1NEAPHARMA Srl

46 4NEOPHARMED GENTILI Srl

47 1Nora Pharma

48 1Novitium Pharma LLC

49 1ORGANON CANADA INC.

50 7Organon

51 1Organon South Africa (Pty) Ltd

52 1PRO DOC LIMITEE

53 1Pensa Pharma

54 1Pharmacare Premium

55 3Pharmascience Inc.

56 2RANBAXY LABORATORIES LIMITED

57 1Radius Health

58 1Ratiopharm GmbH

59 4Rising Pharmaceuticals Inc

60 4S.F.GROUP Srl

61 1SANIS HEALTH INC

62 2SIGMA TAU

63 1SIVEM PHARMACEUTICALS ULC

64 1SO.SE.PHARM Srl

65 6Sandoz B2B

66 4Sun Pharmaceutical Industries Limited

67 1TECNIGEN Srl

68 8Teva Pharmaceutical Industries

69 7Viatris

70 1World Medicine

71 1XL Laboratories Private Limited

72 1Yangtze River Pharmaceutical Group

73 1Zentiva

74 6Zim Laboratories

75 40Blank

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : DMF Available|FDF Compliance-USP

Registration Country : India

Alendronate Sodium

Brand Name :

Dosage Form : DC Granules

Dosage Strength : 70MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : DMF Available|FDF Compliance-USP

Registration Country : India

Octavius Pharma

02

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Antibody Engineering
Not Confirmed
  • 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

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Antibody Engineering
Not Confirmed
  • 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

Antibody Engineering
Not Confirmed
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Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 70MG BASE

Packaging :

Approval Date : 2009-04-22

Application Number : 75871

Regulatory Info : DISCN

Registration Country : USA

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09

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2008-08-04

Application Number : 76768

Regulatory Info : RX

Registration Country : USA

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10

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2008-08-04

Application Number : 76768

Regulatory Info : RX

Registration Country : USA

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11

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 35MG BASE

Packaging :

Approval Date : 2008-08-04

Application Number : 76768

Regulatory Info : RX

Registration Country : USA

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12

Antibody Engineering
Not Confirmed
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Antibody Engineering
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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13

Antibody Engineering
Not Confirmed
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Antibody Engineering
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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14

Antibody Engineering
Not Confirmed
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Antibody Engineering
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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15

Antibody Engineering
Not Confirmed
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Antibody Engineering
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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16

Antibody Engineering
Not Confirmed
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Antibody Engineering
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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17

Antibody Engineering
Not Confirmed
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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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18

Antibody Engineering
Not Confirmed
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Antibody Engineering
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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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19

Antibody Engineering
Not Confirmed
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Antibody Engineering
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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20

Antibody Engineering
Not Confirmed
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Antibody Engineering
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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21

Antibody Engineering
Not Confirmed
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Antibody Engineering
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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22

Antibody Engineering
Not Confirmed
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Antibody Engineering
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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23

Antibody Engineering
Not Confirmed
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Antibody Engineering
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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24

Antibody Engineering
Not Confirmed
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Antibody Engineering
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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25

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2008-08-04

Application Number : 76584

Regulatory Info : DISCN

Registration Country : USA

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26

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2008-08-04

Application Number : 76584

Regulatory Info : DISCN

Registration Country : USA

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27

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 35MG BASE

Packaging :

Approval Date : 2008-08-04

Application Number : 76584

Regulatory Info : DISCN

Registration Country : USA

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28

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 70MG BASE

Packaging :

Approval Date : 2008-08-04

Application Number : 76584

Regulatory Info : DISCN

Registration Country : USA

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29

Antibody Engineering
Not Confirmed
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Antibody Engineering
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 : 76184

Regulatory Info : DISCN

Registration Country : USA

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30

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ALENDRONATE SODIUM

Brand Name : ALENDRONATE SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 35MG BASE

Packaging :

Approval Date : 2008-08-04

Application Number : 76184

Regulatory Info : DISCN

Registration Country : USA

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