01 3APOTEX
02 1AUROBINDO PHARMA LTD
03 1BRIGHT
04 2CHARTWELL RX
05 2COSETTE
06 1ENCUBE
07 4FOUGERA PHARMS
08 12GLAXO GRP LTD
09 6GLAXOSMITHKLINE
10 1GLENMARK PHARMS LTD
11 2HALEON US HOLDINGS
12 7HIKMA
13 3MYLAN
14 1MYLAN SPECIALITY LP
15 1NESHER PHARMS
16 1OPTINOSE US INC
17 4PADAGIS ISRAEL
18 1TARO PHARM INDS
19 14TEVA PHARM
20 3TEVA PHARMS USA
21 1TEVA PHARMS USA INC
01 9AEROSOL, METERED;INHALATION
02 6CREAM;TOPICAL
03 3LOTION;TOPICAL
04 6OINTMENT;TOPICAL
05 32POWDER;INHALATION
06 15SPRAY, METERED;NASAL
01 28DISCN
02 4OTC
03 39RX
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 4ARMONAIR DIGIHALER
08 4ARMONAIR RESPICLICK
09 3AZELASTINE HYDROCHLORIDE AND FLUTICASONE PROPIONATE
10 3CUTIVATE
11 1DYMISTA
12 1FLONASE
13 1FLONASE ALLERGY RELIEF
14 6FLOVENT
15 1FLOVENT DISKUS 100
16 1FLOVENT DISKUS 250
17 1FLOVENT DISKUS 50
18 3FLOVENT HFA
19 20FLUTICASONE PROPIONATE
20 6FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE
21 3WIXELA INHUB
22 1XHANCE
01 38No
02 33Yes
RLD : Yes
TE Code :
Brand Name : CUTIVATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.005% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1990-12-14
Application Number : 19957
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : CUTIVATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1990-12-18
Application Number : 19958
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : FLOVENT
Dosage Form : AEROSOL, METERED;INHALATION
Dosage Strength : 0.044MG/INH
Approval Date : 1996-03-27
Application Number : 20548
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : FLOVENT
Dosage Form : AEROSOL, METERED;INHALATION
Dosage Strength : 0.11MG/INH
Approval Date : 1996-03-27
Application Number : 20548
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : FLOVENT
Dosage Form : AEROSOL, METERED;INHALATION
Dosage Strength : 0.22MG/INH
Approval Date : 1996-03-27
Application Number : 20548
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : FLOVENT
Dosage Form : POWDER;INHALATION
Dosage Strength : 0.044MG/INH
Approval Date : 1997-11-07
Application Number : 20549
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : FLOVENT
Dosage Form : POWDER;INHALATION
Dosage Strength : 0.088MG/INH
Approval Date : 1997-11-07
Application Number : 20549
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : FLOVENT
Dosage Form : POWDER;INHALATION
Dosage Strength : 0.22MG/INH
Approval Date : 1997-11-07
Application Number : 20549
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : FLOVENT DISKUS 50
Dosage Form : POWDER;INHALATION
Dosage Strength : 0.05MG/INH
Approval Date : 2000-09-29
Application Number : 20833
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : FLONASE
Dosage Form : SPRAY, METERED;NASAL
Dosage Strength : 0.05MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1994-10-19
Application Number : 20121
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
