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01 4STRIDES PHARMA INTL
02 7SCHERING
03 2ACERTIS PHARMS
04 2ACTAVIS MID ATLANTIC
05 1AIPING PHARM INC
06 2AIZANT
07 2AM THERAP
08 1AMNEAL IRELAND LTD
09 1AMNEAL PHARMS
10 2AMNEAL PHARMS CO
11 5APOTEX INC
12 2ARMSTRONG PHARMS
13 2AUROBINDO PHARMA LTD
14 2BAUSCH
15 2BOEHRINGER INGELHEIM
16 1CHARTWELL MOLECULAR
17 4CHARTWELL RX
18 3CIPLA
19 4COPLEY PHARM
20 1COSETTE
21 1EPIC PHARMA LLC
22 1GENPHARM
23 8GLAXOSMITHKLINE
24 2HIBROW HLTHCARE
25 1HIKMA
26 1IVAX SUB TEVA PHARMS
27 1KINDEVA
28 1LANDELA PHARM
29 2LEXENPHARM
30 4LUOXIN AUROVITAS
31 1LUPIN
32 1MOVA
33 2MURO
34 2NATCO PHARMA USA
35 6NEPHRON
36 1PADAGIS US
37 4PHARMOBEDIENT
38 3PLIVA
39 1QUAGEN
40 4RISING
41 5RITEDOSE CORP
42 1ROXANE
43 1SANDOZ
44 1SENTISS
45 2SUN PHARM
46 2SUN PHARM INDUSTRIES
47 7TEVA
48 3TEVA BRANDED PHARM
49 2TEVA PHARMS
50 2UCB INC
51 2WARNER CHILCOTT
52 7WATSON LABS
53 1WATSON LABS INC
54 1WATSON LABS TEVA
55 1WOCKHARDT EU OPERATN
56 2ZYDUS PHARMS
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01 17AEROSOL, METERED;INHALATION
02 1CAPSULE;INHALATION
03 2POWDER, METERED;INHALATION
04 1SOLUTION; INHALATION
05 49SOLUTION;INHALATION
06 1SPRAY, METERED;INHALATION
07 12SYRUP;ORAL
08 7TABLET, EXTENDED RELEASE;ORAL
09 47TABLET;ORAL
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01 85DISCN
02 50RX
03 2Blank
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01 2ACCUNEB
02 4ALBUTEROL
03 95ALBUTEROL SULFATE
04 9ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE
05 1ALBUTEROL SULFATE; IPRATROPIUM BROMIDE
06 1COMBIVENT
07 1COMBIVENT RESPIMAT
08 1DUONEB
09 1PROAIR DIGIHALER
10 1PROAIR HFA
11 1PROAIR RESPICLICK
12 7PROVENTIL
13 1PROVENTIL-HFA
14 6VENTOLIN
15 1VENTOLIN HFA
16 1VENTOLIN ROTACAPS
17 2VOLMAX
18 2VOSPIRE ER
01 118No
02 17Yes
03 2Blank
RLD : No
TE Code :
Brand Name : ALBUTEROL SULFATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 4MG BASE
Approval Date : 1989-12-20
Application Number : 72860
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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RLD : No
TE Code :
Brand Name : PROVENTIL
Dosage Form : AEROSOL, METERED;INHALATION
Dosage Strength : 0.09MG/INH
Approval Date : 1982-01-01
Application Number : 17559
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : ALBUTEROL SULFATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 2MG BASE
Approval Date : 1989-12-20
Application Number : 72860
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : VOSPIRE ER
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 4MG BASE
Approval Date : 2002-09-26
Application Number : 76130
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : VOSPIRE ER
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 8MG BASE
Approval Date : 2002-09-26
Application Number : 76130
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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RLD : Yes
TE Code :
Brand Name : PROVENTIL
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-05-07
Application Number : 17853
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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RLD : Yes
TE Code :
Brand Name : PROVENTIL
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-05-07
Application Number : 17853
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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RLD : Yes
TE Code :
Brand Name : PROVENTIL
Dosage Form : SYRUP;ORAL
Dosage Strength : EQ 2MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1983-01-19
Application Number : 18062
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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RLD : Yes
TE Code :
Brand Name : PROVENTIL
Dosage Form : SOLUTION;INHALATION
Dosage Strength : EQ 0.5% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1987-01-14
Application Number : 19243
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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RLD : Yes
TE Code :
Brand Name : PROVENTIL
Dosage Form : SOLUTION;INHALATION
Dosage Strength : EQ 0.083% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1987-01-14
Application Number : 19243
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :