FLOVENT DISKUS- fluticasone propionate powder, metered 
Glaxo Operations UK Ltd

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PRINCIPAL DISPLAY PANEL

NDC 0173-0600-02

FloventDiskus 50 mcg

(fluticasone propionate inhalation powder, 50 mcg)

FOR ORAL INHALATION ONLY

Each blister contains 50 mcg of fluticasone propionate with lactose.

Attention: Dispense with enclosed Patient Information leaflet.

See prescribing information for dosage information.

Rx only

1 Diskus Inhalation Device Containing 1 Foil Strip of 60 Blisters

 
10000000147987 Rev. 10/17
Flovent Diskus 50 mcg 60 dose carton

PRINCIPAL DISPLAY PANEL

NDC 0173-0602-02

FloventDiskus 100 mcg

(fluticasone propionate inhalation powder, 100 mcg)

FOR ORAL INHALATION ONLY

Each blister contains 100 mcg of fluticasone propionate with lactose.

Attention: Dispense with enclosed Patient Information leaflet.

See prescribing information for dosage information.

Rx only

1 Diskus Inhalation Device Containing 1 Foil Strip of 60 Blisters

 
10000000147988 Rev. 10/17
Flovent Diskus 100 mcg 60 dose carton

PRINCIPAL DISPLAY PANEL

NDC 0173-0601-02

FloventDiskus 250 mcg

(fluticasone propionate inhalation powder, 250 mcg)

FOR ORAL INHALATION ONLY

Each blister contains 250 mcg of fluticasone propionate with lactose.

Attention: Dispense with enclosed Patient Information leaflet.

See prescribing information for dosage information.

Rx only

1 Diskus Inhalation Device Containing 1 Foil Strip of 60 Blisters

 
10000000147989 Rev. 10/17
Flovent Diskus 250 mcg 60 dose carton
FLOVENT  DISKUS
fluticasone propionate powder, metered
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:63379-046
Route of AdministrationRESPIRATORY (INHALATION)
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FLUTICASONE PROPIONATE (UNII: O2GMZ0LF5W) (FLUTICASONE - UNII:CUT2W21N7U) FLUTICASONE PROPIONATE100 ug
Inactive Ingredients
Ingredient NameStrength
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63379-046-0260 in 1 INHALER; Type 0: Not a Combination Product10/13/2008
2NDC:63379-046-0028 in 1 INHALER; Type 0: Not a Combination Product10/13/200809/30/2015
3NDC:63379-046-0128 in 1 INHALER; Type 0: Not a Combination Product10/13/2008
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Approved Drug Product Manufactured Under ContractNDA02083310/13/2008
FLOVENT  DISKUS
fluticasone propionate powder, metered
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:63379-047
Route of AdministrationRESPIRATORY (INHALATION)
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FLUTICASONE PROPIONATE (UNII: O2GMZ0LF5W) (FLUTICASONE - UNII:CUT2W21N7U) FLUTICASONE PROPIONATE250 ug
Inactive Ingredients
Ingredient NameStrength
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63379-047-0260 in 1 INHALER; Type 0: Not a Combination Product10/13/2008
2NDC:63379-047-0128 in 1 INHALER; Type 0: Not a Combination Product10/13/2008
3NDC:63379-047-0028 in 1 INHALER; Type 0: Not a Combination Product10/13/200807/31/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Approved Drug Product Manufactured Under ContractNDA02083310/13/2008
FLOVENT  DISKUS
fluticasone propionate powder, metered
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:63379-048
Route of AdministrationRESPIRATORY (INHALATION)
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FLUTICASONE PROPIONATE (UNII: O2GMZ0LF5W) (FLUTICASONE - UNII:CUT2W21N7U) FLUTICASONE PROPIONATE50 ug
Inactive Ingredients
Ingredient NameStrength
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63379-048-0160 in 1 INHALER; Type 0: Not a Combination Product05/08/2007
2NDC:63379-048-0028 in 1 INHALER; Type 0: Not a Combination Product05/08/200712/31/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Approved Drug Product Manufactured Under ContractNDA02083305/08/2007
Labeler - Glaxo Operations UK Ltd (424738227)

Revised: 12/2017
 
Glaxo Operations UK Ltd