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Approved Drug Products containing Prestwick3_000855 listed in the FDA Orange Book. Original Data : FDA Website

Client Email Product
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01 GLAXOSMITHKLINE (3)

02 NORTON WATERFORD (2)

03 SCHERING (5)

04 TEVA BRANDED PHARM (4)

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01 AEROSOL, METERED;INHALATION (7)

02 AEROSOL, METERED;NASAL (4)

03 SPRAY, METERED;NASAL (3)

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01 DISCN (10)

02 RX (4)

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01 BECLOVENT (1)

02 BECONASE (1)

03 BECONASE AQ (1)

04 QNASL (2)

05 QVAR 40 (1)

06 QVAR 80 (1)

07 QVAR REDIHALER (2)

08 VANCENASE (1)

09 VANCENASE AQ (2)

10 VANCERIL (1)

11 VANCERIL DOUBLE STRENGTH (1)

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01 No (7)

02 Yes (7)

URL Supplier Web Content
AEROSOL, METERED;INHALATION
0.042MG/INH
1982-01-01
17573
VANCERIL
DISCN
No
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AEROSOL, METERED;NASAL
0.042MG/INH
1982-01-01
18521
VANCENASE
DISCN
No
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SPRAY, METERED;NASAL
EQ 0.042MG DIPROP/SPRAY
1987-12-23
19589
VANCENASE AQ
DISCN
No
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SPRAY, METERED;NASAL
EQ 0.084MG DIPROP/SPRAY
1996-06-26
20469
VANCENASE AQ
DISCN
No
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AEROSOL, METERED;INHALATION
0.084MG/INH
1996-12-24
20486
VANCERIL DOUBLE STRENG...
DISCN
No
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AEROSOL, METERED;INHALATION
0.042MG/INH
1982-01-01
18153
BECLOVENT
DISCN
No
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AEROSOL, METERED;NASAL
0.042MG/INH
1982-01-01
18584
BECONASE
DISCN
No
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SPRAY, METERED;NASAL
EQ 0.042MG DIPROP/SPRAY
1987-07-27
19389
BECONASE AQ
DISCN
Yes
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AEROSOL, METERED;INHALATION
0.08MG/INH **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
2000-09-15
20911
QVAR 80
DISCN
Yes
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AEROSOL, METERED;INHALATION
0.04MG/INH **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
2000-09-15
20911
QVAR 40
DISCN
Yes
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