01 1ACLIDINIUM BROMIDE
02 1ACLIDINIUM BROMIDE; FORMOTEROL FUMARATE
03 4CICLESONIDE
04 2DIGOXIN
05 1FERUMOXIDES
06 1FERUMOXSIL
07 1FERUMOXYTOL
08 4LOVASTATIN
09 8NISOLDIPINE
10 2OMEPRAZOLE MAGNESIUM
11 1RILUZOLE
01 2AEROSOL, METERED;INHALATION
02 1AEROSOL, METERED;NASAL
03 2FOR SUSPENSION, DELAYED RELEASE;ORAL
04 3INJECTABLE;INJECTION
05 2POWDER, METERED;INHALATION
06 1SOLUTION;INTRAVENOUS
07 1SPRAY, METERED;NASAL
08 1SUSPENSION;ORAL
09 12TABLET, EXTENDED RELEASE;ORAL
10 1TABLET;ORAL
01 10.037MG/INH
02 10.05MG/SPRAY
03 10.08MG/INH
04 10.16MG/INH
05 10.1MG/ML
06 10.25MG/ML
07 10.4MG/INH
08 10.4MG/INH;0.012MG/INH
09 110MG
10 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
11 117MG
12 120MG
13 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
14 125.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
16 134MG
17 140MG
18 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
19 150MG
20 160MG
21 18.5MG
22 1EQ 0.175MG IRON/ML
23 1EQ 10MG BASE/PACKET
24 1EQ 11.2MG IRON/ML
25 1EQ 2.5MG BASE/PACKET
26 1EQ 510MG IRON/17ML (EQ 30MG IRON/ML)
01 13DISCN
02 13RX
RLD : Yes
TE Code :
Dosage Form : POWDER, METERED; INHALATION
Proprietary Name : TUDORZA PRESSAIR
Dosage Strength : 0.4MG/INH
Approval Date : 2012-07-23
Application Number : 202450
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ACLIDINIUM BROMIDE; FORMOTEROL FUMARATE
Dosage Form : POWDER, METERED; INHALATION
Proprietary Name : DUAKLIR PRESSAIR
Dosage Strength : 0.4MG/INH;0.012MG/INH
Approval Date : 2019-03-29
Application Number : 210595
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : AEROSOL, METERED; INHALATION
Proprietary Name : ALVESCO
Dosage Strength : 0.08MG/INH
Approval Date : 2008-01-10
Application Number : 21658
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : AEROSOL, METERED; INHALATION
Proprietary Name : ALVESCO
Dosage Strength : 0.16MG/INH
Approval Date : 2008-01-10
Application Number : 21658
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SPRAY, METERED; NASAL
Proprietary Name : OMNARIS
Dosage Strength : 0.05MG/SPRAY
Approval Date : 2006-10-20
Application Number : 22004
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : AEROSOL, METERED; NASAL
Proprietary Name : ZETONNA
Dosage Strength : 0.037MG/INH
Approval Date : 2012-01-20
Application Number : 202129
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AP
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : LANOXIN
Dosage Strength : 0.25MG/ML
Approval Date : 1982-01-01
Application Number : 9330
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : LANOXIN PEDIATRIC
Dosage Strength : 0.1MG/ML
Approval Date : 1982-01-01
Application Number : 9330
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : FERIDEX I.V.
Dosage Strength : EQ 11.2MG IRON/ML
Approval Date : 1996-08-30
Application Number : 20416
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : SUSPENSION; ORAL
Proprietary Name : GASTROMARK
Dosage Strength : EQ 0.175MG IRON/ML
Approval Date : 1996-12-06
Application Number : 20410
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
