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01 4Orion Corporation

02 3Octavius Pharma Pvt. Ltd

03 12care4 ApS

04 1Abacus Medicine

05 1BB Farma

06 1Beaukev Pharma International

07 3CHEMO

08 2Cipla

09 8Cipla Medpro South Africa

10 1Cross Pharma AB

11 6DOC Generici

12 2Dompe Farmaceutici

13 6EG Spa

14 4ELPEN Pharmaceutical

15 5Farm Agon

16 66GSK

17 9Genetic Spa

18 1Glenmark Pharmaceuticals

19 3Hikma Pharmaceuticals

20 3Macter International Limited

21 3Medisol Lifescience

22 15Menarini

23 4Midas Care Pharmaceuticals

24 3Nobel Ilac Sanayii Ve Ticaret A.S.

25 15ORIFARM GROUP AS

26 1Omnia Pharmaceutical AB

27 3Pharmascience Inc.

28 3SF Group

29 9Sandoz B2B

30 3So.Se.Pharm

31 14Teva Pharmaceutical Industries

32 10Viatris

33 10World Medicine

34 2Zentiva

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PharmaCompass

01

arrow
The Generic Rx Session
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

arrow
The Generic Rx Session
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

arrow
The Generic Rx Session
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

arrow
The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
arrow
arrow
The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
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The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
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The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
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The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
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The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
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The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
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The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
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The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
arrow
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The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
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arrow
The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
arrow
arrow
The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
arrow
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The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
arrow
arrow
The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
arrow
arrow
The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
arrow
arrow
The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
arrow
arrow
The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
arrow
arrow
The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
arrow
arrow
The Generic Rx Session
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

blank

26

The Generic Rx Session
Not Confirmed
arrow
arrow
The Generic Rx Session
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

blank

27

The Generic Rx Session
Not Confirmed
arrow
arrow
The Generic Rx Session
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

blank

28

The Generic Rx Session
Not Confirmed
arrow
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The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
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The Generic Rx Session
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

The Generic Rx Session
Not Confirmed
arrow
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The Generic Rx Session
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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