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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 3CHEMO

09 2Cipla

10 9Cipla Medpro South Africa

11 1Cross Pharma AB

12 6DOC Generici

13 2Dompe Farmaceutici

14 6EG Spa

15 4ELPEN Pharmaceutical

16 5Farm Agon

17 3Forrester Pharma

18 65GSK

19 9Genetic Spa

20 1Glenmark Pharmaceuticals

21 3Hikma Pharmaceuticals

22 3Macter International Limited

23 3Medisol Lifescience

24 15Menarini

25 4Midas Care Pharmaceuticals

26 3Nobel Ilac Sanayii Ve Ticaret A.S.

27 15ORIFARM GROUP AS

28 1Omnia Pharmaceutical AB

29 3Pharmascience Inc.

30 3SF Group

31 11Sandoz B2B

32 3So.Se.Pharm

33 14Teva Pharmaceutical Industries

34 10Viatris

35 10World Medicine

36 2Zentiva

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PharmaCompass

01

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Pharmtech & Ingredients
Not Confirmed

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 :

Dosage Form : Dry Powder for Inhalation

Dosage Strength : 100; 50

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Octavius Pharma

03

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Pharmtech & Ingredients
Not Confirmed

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

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Pharmtech & Ingredients
Not Confirmed

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

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Pharmtech & Ingredients
Not Confirmed

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 :

Dosage Form : Dry Powder for Inhalation

Dosage Strength : 250; 50

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 :

Dosage Form : Dry Powder for Inhalation

Dosage Strength : 500; 50

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Octavius Pharma

08

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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21

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : AIRDUO RESPICLICK

Dosage Form : POWDER;INHALATION

Dosage Strength : 0.232MG/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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22

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : AIRDUO DIGIHALER

Dosage Form : POWDER;INHALATION

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

Packaging :

Approval Date : 2019-07-12

Application Number : 208799

Regulatory Info : DISCN

Registration Country : USA

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23

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : AIRDUO DIGIHALER

Dosage Form : POWDER;INHALATION

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

Packaging :

Approval Date : 2019-07-12

Application Number : 208799

Regulatory Info : DISCN

Registration Country : USA

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24

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : AIRDUO DIGIHALER

Dosage Form : POWDER;INHALATION

Dosage Strength : 0.232MG/INH;EQ 0.014MG BASE/INH

Packaging :

Approval Date : 2019-07-12

Application Number : 208799

Regulatory Info : DISCN

Registration Country : USA

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25

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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 : 2021-12-13

Application Number : 213948

Regulatory Info : RX

Registration Country : USA

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26

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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 : 2021-12-13

Application Number : 213948

Regulatory Info : RX

Registration Country : USA

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27

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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 : 2021-12-13

Application Number : 213948

Regulatory Info : RX

Registration Country : USA

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28

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : WIXELA INHUB

Dosage Form : POWDER;INHALATION

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

Packaging :

Approval Date : 2019-01-30

Application Number : 208891

Regulatory Info : RX

Registration Country : USA

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29

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : WIXELA INHUB

Dosage Form : POWDER;INHALATION

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

Packaging :

Approval Date : 2019-01-30

Application Number : 208891

Regulatory Info : RX

Registration Country : USA

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30

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : WIXELA INHUB

Dosage Form : POWDER;INHALATION

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

Packaging :

Approval Date : 2019-01-30

Application Number : 208891

Regulatory Info : RX

Registration Country : USA

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