01 1TARO PHARM INDS
02 2APOTEX
03 1APOTEX INC
04 1AUROBINDO PHARMA LTD
05 1BRIGHT
06 1CHARTWELL RX
07 2COSETTE
08 1ENCUBE
09 5FOUGERA PHARMS
10 12GLAXO GRP LTD
11 6GLAXOSMITHKLINE
12 1GLENMARK PHARMS LTD
13 2HALEON US HOLDINGS
14 7HIKMA
15 3MYLAN
16 1MYLAN SPECIALITY LP
17 1NESHER PHARMS
18 1OPTINOSE US INC
19 4PADAGIS ISRAEL
20 14TEVA PHARM
21 3TEVA PHARMS USA
01 9AEROSOL, METERED;INHALATION
02 6CREAM;TOPICAL
03 3LOTION;TOPICAL
04 6OINTMENT;TOPICAL
05 32POWDER;INHALATION
06 14SPRAY, METERED;NASAL
01 28DISCN
02 4OTC
03 38RX
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 2AZELASTINE 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 37No
02 33Yes
RLD : No
TE Code :
Brand Name : FLUTICASONE PROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.005%
Approval Date : 2005-06-14
Application Number : 77145
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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Dosage Strength : 0.005% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 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 :
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