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Salmeterol Xinafoate
FDA Orange Book

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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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23 All

01 6GLAXO GRP LTD

02 2GLAXOSMITHKLINE

03 3HIKMA

04 3MYLAN

05 6TEVA PHARM

06 3TEVA PHARMS USA

filter Dosage Reset all filters

23 All

01 4AEROSOL, METERED;INHALATION

02 19POWDER;INHALATION

filter Regulatory Info Reset all filters

23 All

01 4DISCN

02 19RX

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01 1ADVAIR DISKUS 100/50

02 1ADVAIR DISKUS 250/50

03 1ADVAIR DISKUS 500/50

04 3ADVAIR HFA

05 3AIRDUO DIGIHALER

06 3AIRDUO RESPICLICK

07 6FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE

08 2SEREVENT

09 3WIXELA INHUB

filter RLD Reset all filters

23 All

01 10No

02 13Yes

Inke Salmeterol Xinafoate

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01

GLAXOSMITHKLINE

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GLAXOSMITHKLINE

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RLD : No

TE Code :

SALMETEROL XINAFOATE

Brand Name : SEREVENT

Dosage Form : AEROSOL, METERED;INHALATION

Dosage Strength : EQ 0.021MG BASE/INH

Approval Date : 1994-02-04

Application Number : 20236

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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GLAXOSMITHKLINE

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RLD : Yes

TE Code :

SALMETEROL XINAFOATE

Brand Name : SEREVENT

Dosage Form : POWDER;INHALATION

Dosage Strength : EQ 0.05MG BASE/INH

Approval Date : 1997-09-19

Application Number : 20692

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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GLAXO GRP LTD

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RLD : Yes

TE Code : AB

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : ADVAIR DISKUS 100/50

Dosage Form : POWDER;INHALATION

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

Approval Date : 2000-08-24

Application Number : 21077

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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RLD : Yes

TE Code : AB

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : ADVAIR DISKUS 250/50

Dosage Form : POWDER;INHALATION

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

Approval Date : 2000-08-24

Application Number : 21077

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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RLD : Yes

TE Code : AB

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : ADVAIR DISKUS 500/50

Dosage Form : POWDER;INHALATION

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

Approval Date : 2000-08-24

Application Number : 21077

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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GLAXO GRP LTD

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RLD : Yes

TE Code :

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : ADVAIR HFA

Dosage Form : AEROSOL, METERED;INHALATION

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

Approval Date : 2006-06-08

Application Number : 21254

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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GLAXO GRP LTD

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RLD : Yes

TE Code :

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : ADVAIR HFA

Dosage Form : AEROSOL, METERED;INHALATION

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

Approval Date : 2006-06-08

Application Number : 21254

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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GLAXO GRP LTD

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RLD : Yes

TE Code :

FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

Brand Name : ADVAIR HFA

Dosage Form : AEROSOL, METERED;INHALATION

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

Approval Date : 2006-06-08

Application Number : 21254

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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09

HIKMA

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HIKMA

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RLD : No

TE Code : AB

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

Approval Date : 2020-12-17

Application Number : 203433

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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HIKMA

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HIKMA

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RLD : No

TE Code : AB

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

Approval Date : 2020-12-17

Application Number : 203433

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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