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01 1Aspen Pharmacare Holdings

02 1Octavius Pharma Pvt. Ltd

03 12care4

04 2AAIPharma Services Corp.

05 6Actavis Inc

06 4Adcock Ingram

07 1AiPing Pharmaceutical Inc

08 3Aldo-Union

09 2Alphapharm PTY Ltd

10 2Amneal Pharmaceuticals

11 4Apotex Inc

12 1Arrow Pharmaceuticals

13 2Assia Chemical Industries Ltd

14 2Aurobindo Pharma Limited

15 3Bausch & Lomb Incorporated

16 1Beaukev Pharma International

17 42Boehringer Ingelheim GmbH

18 1Cipla

19 5Cipla Medpro South Africa

20 2Deva Holding AS

21 1EG SpA

22 1EG Spa

23 2Farmak JSC

24 1FineTech Pharmaceutical Ltd.

25 1Ha Noi CPC1 Pharmaceutical JSC

26 1Hanlim Pharmaceuticals Inc

27 2Hikma Pharmaceuticals

28 4IBN Savio

29 1Intas Pharmaceuticals

30 1JUNO PHARMACEUTICALS CORP.

31 1KONPHARMA Srl

32 1Konpharma

33 1Lanova Farmaceutici

34 2Luoxin Pharmaceutical

35 2MEDIOLANUM FARMACEUTICI SpA

36 1Medartuum AB

37 2Medisol Lifescience

38 2Medivision

39 1Merck & Co

40 1Midas Care Pharmaceuticals

41 1NATIONAL BIOCHEMISTRY INSTITUTE SAVIO SRL

42 2NORVIUM BIOSCIENCE

43 1Neopharmed Gentili

44 3Nephron Pharmaceuticals Corporation

45 11ORIFARM GROUP AS

46 1PROMEDICA Srl

47 4Paranova Group AS

48 3Pharmachim AB

49 10Pharmascience Inc.

50 1ROXANE

51 1S.F.GROUP Srl

52 2Sun Pharmaceutical Industries Limited

53 15Teva Pharmaceutical Industries

54 2The Ritedose Corporation

55 4VALEAS IND.CHIM.FARMAC. SpA

56 1Valeas

57 4World Medicine

58 1Zennova Pharma

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PharmaCompass

01

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Pharmtech & Ingredients
Not Confirmed

Ipratropium Bromide

Brand Name : Iprabut

Dosage Form : NEB

Dosage Strength : 0.5mg/2.5ml

Packaging : 60X1mg/2.5ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

02

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info :

Registration Country : India

Xylometazoline; Ipratropium Bromide

Brand Name :

Dosage Form : Nasal Spray

Dosage Strength : 0.5MG; 0.6MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Octavius Pharma

03

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 0.02%

Packaging :

Approval Date : 1999-04-22

Application Number : 75111

Regulatory Info : DISCN

Registration Country : USA

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04

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 0.02%

Packaging :

Approval Date : 2005-05-09

Application Number : 76291

Regulatory Info : DISCN

Registration Country : USA

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05

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 0.02%

Packaging :

Approval Date : 2001-03-28

Application Number : 75441

Regulatory Info : DISCN

Registration Country : USA

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06

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.042MG/SPRAY

Packaging :

Approval Date : 2003-04-18

Application Number : 76155

Regulatory Info : RX

Registration Country : USA

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07

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.021MG/SPRAY

Packaging :

Approval Date : 2003-04-18

Application Number : 76156

Regulatory Info : RX

Registration Country : USA

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08

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.021MG/SPRAY

Packaging :

Approval Date : 2003-03-31

Application Number : 75552

Regulatory Info : DISCN

Registration Country : USA

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09

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.042MG/SPRAY

Packaging :

Approval Date : 2003-03-31

Application Number : 75553

Regulatory Info : DISCN

Registration Country : USA

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10

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 0.02%

Packaging :

Approval Date : 2001-10-15

Application Number : 75835

Regulatory Info : DISCN

Registration Country : USA

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11

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.021MG/SPRAY

Packaging :

Approval Date : 2003-03-31

Application Number : 76025

Regulatory Info : RX

Registration Country : USA

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12

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.042MG/SPRAY

Packaging :

Approval Date : 2003-03-31

Application Number : 76103

Regulatory Info : RX

Registration Country : USA

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13

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : ATROVENT

Dosage Form : AEROSOL, METERED;INHALATION

Dosage Strength : 0.018MG/INH

Packaging :

Approval Date : 1986-12-29

Application Number : 19085

Regulatory Info : DISCN

Registration Country : USA

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14

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : ATROVENT

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 0.02% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1993-09-29

Application Number : 20228

Regulatory Info : DISCN

Registration Country : USA

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15

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

Brand Name : COMBIVENT

Dosage Form : AEROSOL, METERED;INHALATION

Dosage Strength : EQ 0.09MG BASE/INH;0.018MG/INH

Packaging :

Approval Date : 1996-10-24

Application Number : 20291

Regulatory Info : DISCN

Registration Country : USA

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16

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : ATROVENT

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.021MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1995-10-20

Application Number : 20393

Regulatory Info : DISCN

Registration Country : USA

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17

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : ATROVENT

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1995-10-20

Application Number : 20394

Regulatory Info : DISCN

Registration Country : USA

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18

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : ATROVENT HFA

Dosage Form : AEROSOL, METERED;INHALATION

Dosage Strength : 0.021MG/INH

Packaging :

Approval Date : 2004-11-27

Application Number : 21527

Regulatory Info : RX

Registration Country : USA

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19

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

Brand Name : COMBIVENT RESPIMAT

Dosage Form : SPRAY, METERED;INHALATION

Dosage Strength : EQ 0.1MG BASE/INH;0.02MG/INH

Packaging :

Approval Date : 2011-10-07

Application Number : 21747

Regulatory Info : RX

Registration Country : USA

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Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.042MG/SPRAY

Packaging :

Approval Date : 2003-11-05

Application Number : 76598

Regulatory Info : RX

Registration Country : USA

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Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.021MG/SPRAY

Packaging :

Approval Date : 2003-11-05

Application Number : 76664

Regulatory Info : RX

Registration Country : USA

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22

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 0.02%

Packaging :

Approval Date : 2001-09-27

Application Number : 75562

Regulatory Info : RX

Registration Country : USA

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23

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

Brand Name : ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.083% BASE;0.017%

Packaging :

Approval Date : 2007-12-31

Application Number : 76749

Regulatory Info : RX

Registration Country : USA

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Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 0.02%

Packaging :

Approval Date : 2002-07-22

Application Number : 75867

Regulatory Info : DISCN

Registration Country : USA

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Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 0.02%

Packaging :

Approval Date : 2000-02-07

Application Number : 75313

Regulatory Info : DISCN

Registration Country : USA

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Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

Brand Name : ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.083% BASE;0.017%

Packaging :

Approval Date : 2007-12-31

Application Number : 76724

Regulatory Info : DISCN

Registration Country : USA

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Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 0.02%

Packaging :

Approval Date : 2001-01-26

Application Number : 75693

Regulatory Info : RX

Registration Country : USA

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28

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 0.02%

Packaging :

Approval Date : 2001-01-19

Application Number : 75507

Regulatory Info : DISCN

Registration Country : USA

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NORVIUM BIOSCIENCE

Country
Pharmtech & Ingredients
Not Confirmed
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NORVIUM BIOSCIENCE

Country
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Pharmtech & Ingredients
Not Confirmed

ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

Brand Name : DUONEB

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.083% BASE;0.017% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2001-03-21

Application Number : 20950

Regulatory Info : DISCN

Registration Country : USA

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NORVIUM BIOSCIENCE

Country
Pharmtech & Ingredients
Not Confirmed
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NORVIUM BIOSCIENCE

Country
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Pharmtech & Ingredients
Not Confirmed

IPRATROPIUM BROMIDE

Brand Name : IPRATROPIUM BROMIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 0.02%

Packaging :

Approval Date : 1997-01-10

Application Number : 74755

Regulatory Info : DISCN

Registration Country : USA

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