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01 4Orion Corporation

02 3Octavius Pharma Pvt. Ltd

03 12care4 ApS

04 1Abacus Medicine

05 3Austell Laboratories

06 1BB Farma

07 1Beaukev Pharma International

08 2Berg Life Sciences

09 3Biodeal Pharmaceuticals

10 3CHEMO

11 2Cipla

12 9Cipla Medpro South Africa

13 1Cross Pharma AB

14 6DOC Generici

15 2Dompe Farmaceutici

16 6EG Spa

17 4ELPEN Pharmaceutical

18 5Farm Agon

19 3Forrester Pharma

20 66GSK

21 9Genetic Spa

22 1Glenmark Pharmaceuticals

23 3Hikma Pharmaceuticals

24 3Loxim Industries

25 3Macter International Limited

26 3Medisol Lifescience

27 15Menarini

28 4Midas Care Pharmaceuticals

29 3Nobel Ilac Sanayii Ve Ticaret A.S.

30 15ORIFARM GROUP AS

31 1Omnia Pharmaceutical AB

32 3Pharmascience Inc.

33 3SF Group

34 11Sandoz B2B

35 3So.Se.Pharm

36 14Teva Pharmaceutical Industries

37 10Viatris

38 10World Medicine

39 2Zentiva

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PharmaCompass

01

Salmeterol/fluticasone

Brand Name : SAFUBREF

Dosage Form : Pressurized Suspension For Inhalation

Dosage Strength : 50 mcg/250 mcg

Packaging : 60 DOSES 50 MCG+250 MCG - RESPIRATORY USE

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Fermion Orion Company 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

Fluticasone Propionate; Salmeterol Xinafoate

Brand Name : Fluticasone Propionate; Salmeterol Xinafoate

Dosage Form : Dry Powder Inhalation

Dosage Strength : 100 MCG; 50MCG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Octavius Pharma

03

Salmeterol/fluticasone

Brand Name : SAFUMIX

Dosage Form : Pressurized Suspension For Inhalation

Dosage Strength : 50 mcg/250 mcg

Packaging : 60 DOSES 50 MCG+250 MCG - RESPIRATORY USE

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Fermion Orion Company Banner

04

Salmeterol/Fluticasone

Brand Name : SAFUBREF

Dosage Form : Pressurized Suspension For Inhalation

Dosage Strength : 50 mcg/500 mcg

Packaging : 60 DOSES 50 MCG+500 MCG - RESPIRATORY USE

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Fermion Orion Company Banner

05

Salmeterol/Fluticasone

Brand Name : SAFUMIX

Dosage Form : Pressurized Suspension For Inhalation

Dosage Strength : 50 mcg/500 mcg

Packaging : 60 DOSES 50 MCG+500 MCG - RESPIRATORY USE

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Fermion Orion Company Banner

06

  • 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

Fluticasone Propionate; Salmeterol Xinafoate

Brand Name : Fluticasone Propionate; Salmeterol Xinafoate

Dosage Form : Dry Powder Inhalation

Dosage Strength : 250 MCG; 50MCG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Octavius Pharma

07

  • 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

Fluticasone Propionate; Salmeterol Xinafoate

Brand Name : Fluticasone Propionate; Salmeterol Xinafoate

Dosage Form : Dry Powder Inhalation

Dosage Strength : 500 MCG; 50MCG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Octavius Pharma

08

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

SALMETEROL XINAFOATE

Brand Name : SEREVENT

Dosage Form : AEROSOL, METERED;INHALATION

Dosage Strength : EQ 0.021MG BASE/INH

Packaging :

Approval Date : 1994-02-04

Application Number : 20236

Regulatory Info : DISCN

Registration Country : USA

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09

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

SALMETEROL XINAFOATE

Brand Name : SEREVENT

Dosage Form : POWDER;INHALATION

Dosage Strength : EQ 0.05MG BASE/INH

Packaging :

Approval Date : 1997-09-19

Application Number : 20692

Regulatory Info : RX

Registration Country : USA

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10

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : ADVAIR DISKUS 100/50

Dosage Form : POWDER;INHALATION

Dosage Strength : 0.1MG/INH;EQ 0.05MG BASE/INH

Packaging :

Approval Date : 2000-08-24

Application Number : 21077

Regulatory Info : RX

Registration Country : USA

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11

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : ADVAIR DISKUS 250/50

Dosage Form : POWDER;INHALATION

Dosage Strength : 0.25MG/INH;EQ 0.05MG BASE/INH

Packaging :

Approval Date : 2000-08-24

Application Number : 21077

Regulatory Info : RX

Registration Country : USA

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12

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : ADVAIR DISKUS 500/50

Dosage Form : POWDER;INHALATION

Dosage Strength : 0.5MG/INH;EQ 0.05MG BASE/INH

Packaging :

Approval Date : 2000-08-24

Application Number : 21077

Regulatory Info : RX

Registration Country : USA

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13

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : ADVAIR HFA

Dosage Form : AEROSOL, METERED;INHALATION

Dosage Strength : 0.045MG/INH;EQ 0.021MG BASE/INH

Packaging :

Approval Date : 2006-06-08

Application Number : 21254

Regulatory Info : RX

Registration Country : USA

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14

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : ADVAIR HFA

Dosage Form : AEROSOL, METERED;INHALATION

Dosage Strength : 0.115MG/INH;EQ 0.021MG BASE/INH

Packaging :

Approval Date : 2006-06-08

Application Number : 21254

Regulatory Info : RX

Registration Country : USA

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15

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : ADVAIR HFA

Dosage Form : AEROSOL, METERED;INHALATION

Dosage Strength : 0.23MG/INH;EQ 0.021MG BASE/INH

Packaging :

Approval Date : 2006-06-08

Application Number : 21254

Regulatory Info : RX

Registration Country : USA

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16

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE

Dosage Form : POWDER;INHALATION

Dosage Strength : 0.1MG/INH;EQ 0.05MG BASE/INH

Packaging :

Approval Date : 2020-12-17

Application Number : 203433

Regulatory Info : RX

Registration Country : USA

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17

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE

Dosage Form : POWDER;INHALATION

Dosage Strength : 0.25MG/INH;EQ 0.05MG BASE/INH

Packaging :

Approval Date : 2020-12-17

Application Number : 203433

Regulatory Info : RX

Registration Country : USA

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18

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE

Dosage Form : POWDER;INHALATION

Dosage Strength : 0.5MG/INH;EQ 0.05MG BASE/INH

Packaging :

Approval Date : 2023-12-19

Application Number : 203433

Regulatory Info : RX

Registration Country : USA

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19

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : AIRDUO RESPICLICK

Dosage Form : POWDER;INHALATION

Dosage Strength : 0.055MG/INH;EQ 0.014MG BASE/INH

Packaging :

Approval Date : 2017-01-27

Application Number : 208799

Regulatory Info : RX

Registration Country : USA

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20

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : AIRDUO RESPICLICK

Dosage Form : POWDER;INHALATION

Dosage Strength : 0.113MG/INH;EQ 0.014MG BASE/INH

Packaging :

Approval Date : 2017-01-27

Application Number : 208799

Regulatory Info : RX

Registration Country : USA

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