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01 2Octavius Pharma Pvt. Ltd

02 1Alembic Pharmaceuticals Limited

03 1Alkem Laboratories

04 3Amneal Pharmaceuticals

05 7Apotex Inc

06 3Aurobindo Pharma Limited

07 1BGP PHARMA ULC

08 2Bayer AG

09 1Bionpharma

10 1Deva Holding AS

11 2Epic Pharma. LLC.

12 1GLAND PHARMA LIMITED

13 2Hanlim Pharmaceuticals Inc

14 2Hikma Pharmaceuticals

15 1Indiana Ophthalmics

16 1Indoco Remedies Limited

17 1Jiangsu Hengrui Medicine

18 1Kolmar Korea Co., Ltd.

19 2Laboratorios Salvat

20 2Loxim Industries

21 2Meda - Asker

22 8Meda AB

23 5Meda Pharmaceuticals Inc.

24 4NORVIUM BIOSCIENCE

25 4ORIFARM GROUP AS

26 1OmniVision GmbH

27 3Padagis

28 1Sandoz B2B

29 1ScieGen Pharmaceuticals

30 1Somerset Pharmaceuticals Inc

31 1Spirig Healthcare

32 2Sun Pharmaceutical Industries Limited

33 1Upsher-Smith Laboratories

34 7Viatris

35 1Viatris Healthcare (Pty) Ltd

36 1Viatris South Africa (Pty) Ltd

37 3World Medicine

38 1Zydus Pharmaceuticals

39 2Blank

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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 :

Registration Country : India

Azelastine Hydrochloride

Brand Name : Azelastine Hydrochloride

Dosage Form : Nasal Spray

Dosage Strength : 0.1%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Octavius Pharma

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

Azelastine Hydrochloride; Fluticasone Propionate

Brand Name : Azelastine Hydrochloride; Fluticasone Propionate

Dosage Form : Nasal Spray

Dosage Strength : 140MCG; 27.5MCG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Octavius Pharma

03

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 0.05%

Packaging :

Approval Date : 2019-03-20

Application Number : 209620

Regulatory Info : RX

Registration Country : USA

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04

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.137MG/SPRAY

Packaging :

Approval Date : 2017-08-18

Application Number : 208156

Regulatory Info : RX

Registration Country : USA

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05

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.137MG/SPRAY

Packaging :

Approval Date : 2017-08-28

Application Number : 204660

Regulatory Info : RX

Registration Country : USA

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06

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.2055MG/SPRAY

Packaging :

Approval Date : 2017-12-15

Application Number : 208199

Regulatory Info : DISCN

Registration Country : USA

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07

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.137MG/SPRAY

Packaging :

Approval Date : 2009-04-30

Application Number : 77954

Regulatory Info : RX

Registration Country : USA

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08

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 0.05%

Packaging :

Approval Date : 2009-08-03

Application Number : 78621

Regulatory Info : RX

Registration Country : USA

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09

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.2055MG/SPRAY

Packaging :

Approval Date : 2012-08-31

Application Number : 201846

Regulatory Info : DISCN

Registration Country : USA

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10

BePharma
Not Confirmed
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BePharma
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AZELASTINE HYDROCHLORIDE; FLUTICASONE PROPIONATE

Brand Name : AZELASTINE HYDROCHLORIDE AND FLUTICASONE PROPIONATE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.137MG/SPRAY;0.05MG/SPRAY

Packaging :

Approval Date : 2017-04-28

Application Number : 207712

Regulatory Info : RX

Registration Country : USA

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11

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.137MG/SPRAY

Packaging :

Approval Date : 2015-07-28

Application Number : 90176

Regulatory Info : DISCN

Registration Country : USA

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12

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 0.05%

Packaging :

Approval Date : 2016-11-08

Application Number : 203660

Regulatory Info : DISCN

Registration Country : USA

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13

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.137MG/SPRAY

Packaging :

Approval Date : 2019-05-17

Application Number : 207610

Regulatory Info : RX

Registration Country : USA

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14

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.137MG/SPRAY

Packaging :

Approval Date : 2014-10-24

Application Number : 91444

Regulatory Info : DISCN

Registration Country : USA

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15

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.2055MG/SPRAY

Packaging :

Approval Date : 2017-09-22

Application Number : 207243

Regulatory Info : DISCN

Registration Country : USA

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16

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHRLORIDE

Brand Name : ASTEPRO

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.1%

Packaging :

Approval Date :

Application Number : 22371

Regulatory Info :

Registration Country : USA

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17

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHRLORIDE

Brand Name : ASTEPRO

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.15%

Packaging :

Approval Date :

Application Number : 22371

Regulatory Info :

Registration Country : USA

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18

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.2055MG/SPRAY

Packaging :

Approval Date : 2014-05-08

Application Number : 202743

Regulatory Info : DISCN

Registration Country : USA

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19

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE; FLUTICASONE PROPIONATE

Brand Name : AZELASTINE HYDROCHLORIDE AND FLUTICASONE PROPIONATE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.137MG/SPRAY;0.05MG/SPRAY

Packaging :

Approval Date : 2021-02-18

Application Number : 208111

Regulatory Info : RX

Registration Country : USA

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20

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 0.05%

Packaging :

Approval Date : 2012-05-31

Application Number : 202305

Regulatory Info : RX

Registration Country : USA

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21

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 0.05%

Packaging :

Approval Date : 2019-03-29

Application Number : 207411

Regulatory Info : RX

Registration Country : USA

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22

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 0.05%

Packaging :

Approval Date : 2010-06-21

Application Number : 78738

Regulatory Info : DISCN

Registration Country : USA

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23

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.137MG/SPRAY

Packaging :

Approval Date : 2012-05-23

Application Number : 90423

Regulatory Info : DISCN

Registration Country : USA

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24

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.137MG/SPRAY

Packaging :

Approval Date : 2017-03-17

Application Number : 202609

Regulatory Info : RX

Registration Country : USA

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25

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE; FLUTICASONE PROPIONATE

Brand Name : DYMISTA

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.137MG/SPRAY;0.05MG/SPRAY

Packaging :

Approval Date : 2012-05-01

Application Number : 202236

Regulatory Info : RX

Registration Country : USA

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26

BePharma
Not Confirmed
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : AZELASTINE HYDROCHLORIDE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.137MG/SPRAY

Packaging :

Approval Date : 2017-08-14

Application Number : 91409

Regulatory Info : RX

Registration Country : USA

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27

NORVIUM BIOSCIENCE

Country
BePharma
Not Confirmed
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NORVIUM BIOSCIENCE

Country
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : ASTELIN

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.137MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1996-11-01

Application Number : 20114

Regulatory Info : DISCN

Registration Country : USA

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28

NORVIUM BIOSCIENCE

Country
BePharma
Not Confirmed
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NORVIUM BIOSCIENCE

Country
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : OPTIVAR

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2000-05-22

Application Number : 21127

Regulatory Info : DISCN

Registration Country : USA

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29

NORVIUM BIOSCIENCE

Country
BePharma
Not Confirmed
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NORVIUM BIOSCIENCE

Country
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : ASTEPRO

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.137MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2008-10-15

Application Number : 22203

Regulatory Info : DISCN

Registration Country : USA

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30

NORVIUM BIOSCIENCE

Country
BePharma
Not Confirmed
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NORVIUM BIOSCIENCE

Country
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BePharma
Not Confirmed

AZELASTINE HYDROCHLORIDE

Brand Name : ASTEPRO

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.2055MG/SPRAY

Packaging :

Approval Date : 2009-08-31

Application Number : 22203

Regulatory Info : DISCN

Registration Country : USA

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