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Salmeterol Xinafoate
Canada

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Salmeterol Xinafoate

ACCESS ALL DATA, CHEMISTRY

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CHEMISTRY
Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

40 API Suppliers, 20 USDMF, 16 CEP/COS, 1 JDMF, 11 EU WC, 12 NDC API, 28 Listed Suppliers, $ API Reference Price

40 API Suppliers
20 USDMF
16 CEP/COS
1 JDMF
11 EU WC
12 NDC API
28 Listed Suppliers
$ API Reference Price

DEVELOPMENTS

10 Drugs in Development

10 Drugs in Development

INTERMEDIATES

11 Intermediates Suppliers

11 Intermediates Suppliers

FINISHED DOSAGE FORMULATIONS

233 FDF Dossiers, 23 FDA Orange Book, 143 Europe, 12 Canada, 1 Australia, 31 South Africa, 23 Listed Dossiers

233 FDF Dossiers
23 FDA Orange Book
143 Europe
12 Canada
1 Australia
31 South Africa
23 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

POWDER;INHALATION - 0.055MG/INH;EQ 0.014MG BASE/INH, POWDER;INHALATION - 0.113MG/INH;EQ 0.014MG BASE/INH, POWDER;INHALATION - 0.232MG/INH;EQ 0.014MG BASE/INH, POWDER;INHALATION - 0.1MG/INH;EQ 0.05MG BASE/INH, POWDER;INHALATION - 0.25MG/INH;EQ 0.05MG BASE/INH, POWDER;INHALATION - 0.5MG/INH;EQ 0.05MG BASE/INH, AEROSOL, METERED;INHALATION - 0.045MG/INH;EQ 0.021MG BASE/INH, AEROSOL, METERED;INHALATION - 0.115MG/INH;EQ 0.021MG BASE/INH, AEROSOL, METERED;INHALATION - 0.23MG/INH;EQ 0.021MG BASE/INH

POWDER;INHALATION - 0.055MG/INH;EQ 0.014MG BASE/INH
POWDER;INHALATION - 0.113MG/INH;EQ 0.014MG BASE/INH
POWDER;INHALATION - 0.232MG/INH;EQ 0.014MG BASE/INH
POWDER;INHALATION - 0.1MG/INH;EQ 0.05MG BASE/INH
POWDER;INHALATION - 0.25MG/INH;EQ 0.05MG BASE/INH
POWDER;INHALATION - 0.5MG/INH;EQ 0.05MG BASE/INH
AEROSOL, METERED;INHALATION - 0.045MG/INH;EQ 0.021MG BASE/INH
AEROSOL, METERED;INHALATION - 0.115MG/INH;EQ 0.021MG BASE/INH
AEROSOL, METERED;INHALATION - 0.23MG/INH;EQ 0.021MG BASE/INH

RELATED EXCIPIENT COMPANIES

1 Faran Shimi Pharmaceutical, 3 Gangwal Healthcare, 1 Nanjing Well Pharmaceutical, 2 BASF, 2 DFE Pharma, 17 Kerry, 2 Microlex e.U, 1 Pluviaendo, 1 Roquette, 2 Sigachi Industries

1 Faran Shimi Pharmaceutical
3 Gangwal Healthcare
1 Nanjing Well Pharmaceutical
2 BASF
2 DFE Pharma
17 Kerry
2 Microlex e.U
1 Pluviaendo
1 Roquette
2 Sigachi Industries

EXCIPIENTS BY APPLICATIONS

21 Fillers, Diluents & Binders, 9 Direct Compression, 7 Co-Processed Excipients, 6 Granulation, 1 Coating Systems & Additives, 1 Controlled & Modified Release, 1 Parenteral

21 Fillers, Diluents & Binders
9 Direct Compression
7 Co-Processed Excipients
6 Granulation
1 Coating Systems & Additives
1 Controlled & Modified Release
1 Parenteral

DIGITAL CONTENT

8 DATA COMPILATION #PharmaFlow, 80 NEWS #PharmaBuzz

8 DATA COMPILATION #PharmaFlow
80 NEWS #PharmaBuzz

GLOBAL SALES INFORMATION

1 US Medicaid Prescriptions, 125 Finished Drug Prices, 5 Annual Reports

1 US Medicaid Prescriptions
125 Finished Drug Prices
5 Annual Reports

MARKET PLACE

4 APIs, 2 FDF Dossiers

4 APIs
2 FDF Dossiers

PATENTS & EXCLUSIVITIES

247 US Patents, 4 US Exclusivities, 14 Health Canada Patents

247 US Patents
4 US Exclusivities
14 Health Canada Patents

REF. STANDARDS & IMPURITIES

3 EDQM, 6 USP, 7 Others

3 EDQM
6 USP
7 Others

$ API Ref.Price (USD/KG) : 39,700 Xls

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12 All

01 6GLAXOSMITHKLINE INC

02 3MYLAN PHARMACEUTICALS ULC

03 3PHARMASCIENCE INC

filter Active Ingredients Reset all filters

12 All

01 12SALMETEROL (SALMETEROL XINAFOATE)

filter Dosage Form Reset all filters

12 All

01 2AEROSOL, METERED DOSE

02 10POWDER

filter Brand Name Reset all filters

12 All

01 1ADVAIR 100 DISKUS

02 1ADVAIR 125

03 1ADVAIR 250

04 1ADVAIR 250 DISKUS

05 1ADVAIR 500 DISKUS

06 3PMS-FLUTICASONE PROPIONATE/SALMETEROL DPI

07 1SEREVENT DISKUS (50MCG/DOSE)

08 3WIXELA INHUB

Inke Salmeterol Xinafoate

List of Suppliers

Product Main Page

01

GLAXOSMITHKLINE INC

Pharmtech & Ingredients

Not Confirmed

GLAXOSMITHKLINE INC

Pharmtech & Ingredients

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Regulatory Info : Prescription

Registration Country : Canada

SALMETEROL (SALMETEROL XINAFOATE)

Brand Name : ADVAIR 100 DISKUS

Dosage Form : POWDER

Dosage Strength : 50MCG/ACT

Packaging : 28,60 DOSES

Approval Date :

Application Number : 2240835

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

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Digital Content

Corporate PDF

02

GLAXOSMITHKLINE INC

Pharmtech & Ingredients

Not Confirmed

GLAXOSMITHKLINE INC

Pharmtech & Ingredients

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Regulatory Info : Prescription

Registration Country : Canada

SALMETEROL (SALMETEROL XINAFOATE)

Brand Name : ADVAIR 250 DISKUS

Dosage Form : POWDER

Dosage Strength : 50MCG/ACT

Packaging : 28,60 DOSES

Approval Date :

Application Number : 2240836

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

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03

GLAXOSMITHKLINE INC

Pharmtech & Ingredients

Not Confirmed

GLAXOSMITHKLINE INC

Pharmtech & Ingredients

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Regulatory Info : Prescription

Registration Country : Canada

SALMETEROL (SALMETEROL XINAFOATE)

Brand Name : ADVAIR 500 DISKUS

Dosage Form : POWDER

Dosage Strength : 50MCG/ACT

Packaging : 28,60 DOSES

Approval Date :

Application Number : 2240837

Regulatory Info : Prescription

Registration Country : Canada

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04

GLAXOSMITHKLINE INC

Pharmtech & Ingredients

Not Confirmed

GLAXOSMITHKLINE INC

Pharmtech & Ingredients

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Regulatory Info : Prescription

Registration Country : Canada

SALMETEROL (SALMETEROL XINAFOATE)

Brand Name : SEREVENT DISKUS (50MCG/DOSE)

Dosage Form : POWDER

Dosage Strength : 50MCG/ACT

Packaging : 60 DOSE

Approval Date :

Application Number : 2231129

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

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05

GLAXOSMITHKLINE INC

Pharmtech & Ingredients

Not Confirmed

GLAXOSMITHKLINE INC

Pharmtech & Ingredients

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Regulatory Info : Prescription

Registration Country : Canada

SALMETEROL (SALMETEROL XINAFOATE)

Brand Name : ADVAIR 125

Dosage Form : AEROSOL, METERED DOSE

Dosage Strength : 25MCG/ACT

Packaging : 120 DOSES

Approval Date :

Application Number : 2245126

Regulatory Info : Prescription

Registration Country : Canada

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Product Web Link

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06

GLAXOSMITHKLINE INC

Pharmtech & Ingredients

Not Confirmed

GLAXOSMITHKLINE INC

Pharmtech & Ingredients

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

SALMETEROL (SALMETEROL XINAFOATE)

Brand Name : ADVAIR 250

Dosage Form : AEROSOL, METERED DOSE

Dosage Strength : 25MCG/ACT

Packaging : 120 DOSES

Approval Date :

Application Number : 2245127

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

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07

PHARMASCIENCE INC

Pharmtech & Ingredients

Not Confirmed

PHARMASCIENCE INC

Pharmtech & Ingredients

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Regulatory Info : Prescription

Registration Country : Canada

SALMETEROL (SALMETEROL XINAFOATE)

Brand Name : PMS-FLUTICASONE PROPIONATE/SALMETEROL DPI

Dosage Form : POWDER

Dosage Strength : 50MCG/ACT

Packaging :

Approval Date :

Application Number : 2494507

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

08

PHARMASCIENCE INC

Pharmtech & Ingredients

Not Confirmed

PHARMASCIENCE INC

Pharmtech & Ingredients

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

SALMETEROL (SALMETEROL XINAFOATE)

Brand Name : PMS-FLUTICASONE PROPIONATE/SALMETEROL DPI

Dosage Form : POWDER

Dosage Strength : 50MCG/ACT

Packaging :

Approval Date :

Application Number : 2494523

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

09

PHARMASCIENCE INC

Pharmtech & Ingredients

Not Confirmed

PHARMASCIENCE INC

Pharmtech & Ingredients

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

SALMETEROL (SALMETEROL XINAFOATE)

Brand Name : PMS-FLUTICASONE PROPIONATE/SALMETEROL DPI

Dosage Form : POWDER

Dosage Strength : 50MCG/ACT

Packaging :

Approval Date :

Application Number : 2494515

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

10

MYLAN PHARMACEUTICALS ULC

Pharmtech & Ingredients

Not Confirmed

MYLAN PHARMACEUTICALS ULC

Pharmtech & Ingredients

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Regulatory Info : Prescription

Registration Country : Canada

SALMETEROL (SALMETEROL XINAFOATE)

Brand Name : WIXELA INHUB

Dosage Form : POWDER

Dosage Strength : 50MCG/ACT

Packaging :

Approval Date :

Application Number : 2495597

Regulatory Info : Prescription

Registration Country : Canada

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